A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518651



Internal ID15445944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2117681..2129624hg38UCSC Ensembl
Innerchr5:2117795..2129738hg19UCSC Ensembl
Innerchr5:2170795..2182738hg18UCSC Ensembl
Innerchr5:2170795..2182738hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3811944
hg1911944
hg1811944
hg1711944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696100
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518651
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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