A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589293



Internal ID16030016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:356048..433324hg38UCSC Ensembl
Innerchr3:397731..475007hg19UCSC Ensembl
Innerchr3:372731..450007hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3877277
hg1977277
hg1877277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957804
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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