A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698966



Internal ID15435618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140626845..140628834hg38UCSC Ensembl
Innerchr5:140006430..140008419hg19UCSC Ensembl
Innerchr5:139986614..139988603hg18UCSC Ensembl
Innerchr5:139986614..139988603hg17UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381990
hg191990
hg181990
hg171990
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523239
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698966
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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