A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697319



Internal ID15087285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134530651..134569277hg38UCSC Ensembl
Innerchr7:134215403..134254029hg19UCSC Ensembl
Innerchr7:133865943..133904569hg18UCSC Ensembl
Innerchr7:133672658..133711284hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3838627
hg1938627
hg1838627
hg1738627
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520274
Supporting Variants
Samples
Known GenesAKR1B10, AKR1B15
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697319
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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