A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705485



Internal ID15442137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:101088377..101882383hg38UCSC Ensembl
Innerchr5:100424081..101218087hg19UCSC Ensembl
Innerchr5:100451980..101245986hg18UCSC Ensembl
Innerchr5:100451980..101245986hg17UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38794007
hg19794007
hg18794007
hg17794007
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528811
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705485
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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