A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591274



Internal ID16378683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110564869..110602188hg38UCSC Ensembl
Innerchr3:110283716..110321035hg19UCSC Ensembl
Innerchr3:111766406..111803725hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3837320
hg1937320
hg1837320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152525
SamplesHGDP01103
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591274
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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