A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589247



Internal ID16029970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:181998..209030hg38UCSC Ensembl
Innerchr3:223681..250713hg19UCSC Ensembl
Innerchr3:198681..225713hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3827033
hg1927033
hg1827033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957556
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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