A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520187



Internal ID15447480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66803291..66808513hg38UCSC Ensembl
Innerchr15:67095629..67100851hg19UCSC Ensembl
Innerchr15:64882683..64887905hg18UCSC Ensembl
Innerchr15:64882683..64887905hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385223
hg195223
hg185223
hg175223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675084, nssv661512, nssv685417, nssv687399, nssv702377, nssv683686
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520187
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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