A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528867



Internal ID15456160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8913275..8953502hg38UCSC Ensembl
Innerchr3:8954959..8995186hg19UCSC Ensembl
Innerchr3:8929959..8970186hg18UCSC Ensembl
Innerchr3:8929959..8970186hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3840228
hg1940228
hg1840228
hg1740228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705547
Samples
Known GenesRAD18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528867
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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