A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589291



Internal ID16030014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:278518..1087112hg38UCSC Ensembl
Innerchr3:320201..1128796hg19UCSC Ensembl
Innerchr3:295201..1103796hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38808595
hg19808596
hg18808596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957802
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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