A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701163



Internal ID15091129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80361713..80372907hg38UCSC Ensembl
Innerchr7:79991029..80002223hg19UCSC Ensembl
Innerchr7:79828965..79840159hg18UCSC Ensembl
Innerchr7:79635680..79646874hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3811195
hg1911195
hg1811195
hg1711195
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525104
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701163
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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