Hs02932239_cn

• Gene Symbol: ANKRD13D
• Assay Reference Genome Location: Chr.11:67301108 on build GRCh38
• Cytoband: 11q13.2

Target Gene Details

• Entrez Gene ID: 338692
• Gene Name: ankyrin repeat domain 13D
• Gene Aliases: -
• Location: Chr.11:67289291-67302484 on Build GRCh38
• Assay Gene Location: Overlaps Exon 13 - Intron 13

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ANKRD13D	NM_207354.2			NP_997237.2
	NR_030767.1
	XM_011544985.1			XP_011543287.1
	XM_011544986.1			XP_011543288.1
	XM_011544987.2			XP_011543289.1
	XM_011544988.2			XP_011543290.1
	AK027313.1
	AK057566.1
	AK057681.1
	AK091614.1
	AK096277.1
	AK124721.1			BAC85932.1
	AK126438.1			BAC86550.1
	BC044239.1			AAH44239.1
	BC110419.1
	BC121024.1
	BC121025.2

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv555253	Chr.11:67265605 - 67397024 on Build GRCh38	Loss	POLD4 SSH3 GRK2 CLCF1 RAD9A ANKRD13D LOC100130987

More Information

Additional Information:

For this assay, SNP(s) [rs76948867] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Non-exonic, DGV Variation