A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698997



Internal ID15435649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44089694..44150749hg38UCSC Ensembl
Innerchr4:44091711..44152766hg19UCSC Ensembl
Innerchr4:43786468..43847523hg18UCSC Ensembl
Innerchr4:43932639..43993694hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3861056
hg1961056
hg1861056
hg1761056
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523263
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698997
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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