A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528880



Internal ID15456173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:42940128..42967113hg38UCSC Ensembl
Innerchr5:42940230..42967215hg19UCSC Ensembl
Innerchr5:42975987..43002972hg18UCSC Ensembl
Innerchr5:42975987..43002972hg17UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3826986
hg1926986
hg1826986
hg1726986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705560
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528880
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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