A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026121



Internal ID19115338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:34819110..34993583hg38UCSC Ensembl
Innerchr6:34786887..34961360hg19UCSC Ensembl
Innerchr6:34894865..35069338hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38174474
hg19174474
hg18174474
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657374
Samples
Known GenesANKS1A, TAF11, UHRF1BP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026121
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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