A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669413



Internal ID15406065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101325082..101325252hg38UCSC Ensembl
Innerchr7:100968363..100968533hg19UCSC Ensembl
Innerchr7:100755083..100755253hg18UCSC Ensembl
Innerchr7:100561798..100561968hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38171
hg19171
hg18171
hg17171
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517175
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669413
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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