A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700113



Internal ID15436765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119653363..119966578hg38UCSC Ensembl
Innerchr7:119293417..119606632hg19UCSC Ensembl
Innerchr7:119080653..119393868hg18UCSC Ensembl
Innerchr7:118887368..119200583hg17UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38313216
hg19313216
hg18313216
hg17313216
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524225
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700113
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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