A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569684



Internal ID16357093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62414416..62415455hg38UCSC Ensembl
Innerchr15:62706615..62707654hg19UCSC Ensembl
Innerchr15:60493907..60494946hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381040
hg191040
hg181040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4568n54
Supporting Variantsnssv843928, nssv843927
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569684
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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