A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591271



Internal ID16378680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110159161..110325754hg38UCSC Ensembl
Innerchr3:109878008..110044601hg19UCSC Ensembl
Innerchr3:111360698..111527291hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38166594
hg19166594
hg18166594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971492
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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