A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705010



Internal ID15441662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:157066729..157078222hg38UCSC Ensembl
Innerchr5:156493740..156505233hg19UCSC Ensembl
Innerchr5:156426318..156437811hg18UCSC Ensembl
Innerchr5:156426318..156437811hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3811494
hg1911494
hg1811494
hg1711494
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528418
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705010
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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