A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696678



Internal ID15086644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76270093..76317446hg38UCSC Ensembl
Innerchr7:75899411..75946763hg19UCSC Ensembl
Innerchr7:75737347..75784699hg18UCSC Ensembl
Innerchr7:75544062..75591414hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3847354
hg1947353
hg1847353
hg1747353
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519194
Supporting Variants
Samples
Known GenesHSPB1, SRRM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696678
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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