A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv837282



Internal ID16131238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20389712..20418387hg38UCSC Ensembl
Innerchr15:20594965..20623640hg19UCSC Ensembl
Innerchr15:18854979..18883654hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3828676
hg1928676
hg1828676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv567451
Supporting Variants
Samples
Known GenesHERC2P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv837282
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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