A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569678



Internal ID16357087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62414313..62415372hg38UCSC Ensembl
Innerchr15:62706512..62707571hg19UCSC Ensembl
Innerchr15:60493804..60494863hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381060
hg191060
hg181060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4568n54
Supporting Variantsnssv843909, nssv843910
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569678
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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