A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039813



Internal ID19129032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..20411461hg38UCSC Ensembl
Innerchr15:20581550..20616714hg19UCSC Ensembl
Innerchr15:18841564..18876728hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3835165
hg1935165
hg1835165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2274n100
Supporting Variantsnssv3714564, nssv3535921
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)nsv1039813
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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