A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660140



Internal ID15396792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:46212088..46227015hg38UCSC Ensembl
Innerchr7:46251686..46266613hg19UCSC Ensembl
Innerchr7:46218211..46233138hg18UCSC Ensembl
Innerchr7:46024926..46039853hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3814928
hg1914928
hg1814928
hg1714928
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520026
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660140
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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