A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699240



Internal ID15435892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110098190..110143083hg38UCSC Ensembl
Innerchr5:109433891..109478784hg19UCSC Ensembl
Innerchr5:109461790..109506683hg18UCSC Ensembl
Innerchr5:109461790..109506683hg17UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3844894
hg1944894
hg1844894
hg1744894
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523477
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699240
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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