A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668162



Internal ID15058128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:77478148..77492871hg38UCSC Ensembl
Innerchr7:77107465..77122188hg19UCSC Ensembl
Innerchr7:76945401..76960124hg18UCSC Ensembl
Innerchr7:76752116..76766839hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3814724
hg1914724
hg1814724
hg1714724
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516408
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668162
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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