A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589889



Internal ID16377298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21215817..21304147hg38UCSC Ensembl
Innerchr3:21257309..21345639hg19UCSC Ensembl
Innerchr3:21232313..21320643hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3888331
hg1988331
hg1888331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8256n54
Supporting Variantsnssv1151754, nssv959915, nssv959914, nssv1151753, nssv959913
SamplesHGDP01063, HGDP01067
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589889
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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