A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3537511



Internal ID18835792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359322..20411461hg38UCSC Ensembl
Innerchr15:20564575..20616714hg19UCSC Ensembl
Innerchr15:18824589..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3852140
hg1952140
hg1852140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039708
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)nssv3537511
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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