A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515785



Internal ID15442842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:53221752..53333771hg38UCSC Ensembl
Innerchr10:54981512..55093531hg19UCSC Ensembl
Innerchr10:54651518..54763537hg18UCSC Ensembl
Innerchr10:54651518..54763537hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38112020
hg19112020
hg18112020
hg17112020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653050, nssv652109
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515785
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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