A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523782



Internal ID15451075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2625719..2641408hg38UCSC Ensembl
Innerchr5:2625833..2641522hg19UCSC Ensembl
Innerchr5:2678833..2694522hg18UCSC Ensembl
Innerchr5:2678833..2694522hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3815690
hg1915690
hg1815690
hg1715690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699607
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523782
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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