A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699568



Internal ID15436220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:94751197..94777113hg38UCSC Ensembl
Innerchr7:94380509..94406425hg19UCSC Ensembl
Innerchr7:94218445..94244361hg18UCSC Ensembl
Innerchr7:94025160..94051076hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825917
hg1925917
hg1825917
hg1725917
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523751
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699568
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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