A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713620



Internal ID19011901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240873..20411461hg38UCSC Ensembl
Innerchr15:20446126..20616714hg19UCSC Ensembl
Innerchr15:18706140..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38170589
hg19170589
hg18170589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049017
Supporting Variants
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713620
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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