A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694132



Internal ID15084098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:99703135..99717363hg38UCSC Ensembl
Innerchr7:99300758..99314986hg19UCSC Ensembl
Innerchr7:99138694..99152922hg18UCSC Ensembl
Innerchr7:98945409..98959637hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3814229
hg1914229
hg1814229
hg1714229
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522107
Supporting Variants
Samples
Known GenesCYP3A7, CYP3A7-CYP3AP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694132
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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