A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589277



Internal ID16376686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188773..193043hg38UCSC Ensembl
Innerchr3:230456..234726hg19UCSC Ensembl
Innerchr3:205456..209726hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg384271
hg194271
hg184271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8149n54
Supporting Variantsnssv957786
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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