A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713309



Internal ID18664904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110581726..111040647hg38UCSC Ensembl
Innerchr13:111234073..111692994hg19UCSC Ensembl
Innerchr13:110032074..110490995hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38458922
hg19458922
hg18458922
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044340
Supporting Variants
Samples
Known GenesANKRD10, CARKD, CARS2, ING1, LINC00346
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713309
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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