A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589424



Internal ID16030147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051682..4055139hg38UCSC Ensembl
Innerchr3:4093366..4096823hg19UCSC Ensembl
Innerchr3:4068366..4071823hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg383458
hg193458
hg183458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958023
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589424
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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