A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523725



Internal ID15451018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:87035931..87055061hg38UCSC Ensembl
Innerchr5:86331748..86350878hg19UCSC Ensembl
Innerchr5:86367504..86386634hg18UCSC Ensembl
Innerchr5:86367504..86386634hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3819131
hg1919131
hg1819131
hg1719131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699541
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523725
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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