A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527643



Internal ID15454936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138244561..138269674hg38UCSC Ensembl
Innerchr7:137929307..137954419hg19UCSC Ensembl
Innerchr7:137579847..137604959hg18UCSC Ensembl
Innerchr7:137386562..137411674hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3825114
hg1925113
hg1825113
hg1725113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704114
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527643
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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