A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3497681



Internal ID19085322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5610776..5675162hg38UCSC Ensembl
Innerchr10:5652739..5717125hg19UCSC Ensembl
Innerchr10:5692745..5757131hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3864387
hg1964387
hg1864387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037709
Supporting Variants
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3497681
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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