A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589506



Internal ID16376915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:5754531..6220792hg38UCSC Ensembl
Innerchr3:5796218..6262479hg19UCSC Ensembl
Innerchr3:5771218..6237479hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38466262
hg19466262
hg18466262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152473
SamplesHGDP01347
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589506
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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