A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519319



Internal ID15446612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99432456..99451301hg38UCSC Ensembl
Innerchr15:99972661..99991506hg19UCSC Ensembl
Innerchr15:97790184..97809029hg18UCSC Ensembl
Innerchr15:97790184..97809029hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3818846
hg1918846
hg1818846
hg1718846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692748, nssv655400
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519319
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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