A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652109



Internal ID15388761
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515785
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652109
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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