A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589411



Internal ID16376820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4032349..4124049hg38UCSC Ensembl
Innerchr3:4074033..4165733hg19UCSC Ensembl
Innerchr3:4049033..4140733hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3891701
hg1991701
hg1891701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8175n54
Supporting Variantsnssv1152447
SamplesHGDP01333
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589411
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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