A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536294



Internal ID18834575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20344625..20422227hg38UCSC Ensembl
Innerchr15:20549878..20627480hg19UCSC Ensembl
Innerchr15:18809892..18887494hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3877603
hg1977603
hg1877603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044039
Supporting Variants
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536294
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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