A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589625



Internal ID16377034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784055..8812681hg38UCSC Ensembl
Innerchr3:8825741..8854367hg19UCSC Ensembl
Innerchr3:8800741..8829367hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3828627
hg1928627
hg1828627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv1151845
SamplesHGDP01380
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589625
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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