A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538688



Internal ID18836969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381218..20411461hg38UCSC Ensembl
Innerchr15:20586471..20616714hg19UCSC Ensembl
Innerchr15:18846485..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3830244
hg1930244
hg1830244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051604
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)nssv3538688
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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