A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590026



Internal ID16030749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:29246160..29579113hg38UCSC Ensembl
Innerchr3:29287651..29620604hg19UCSC Ensembl
Innerchr3:29262655..29595608hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38332954
hg19332954
hg18332954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960941
Samples
Known GenesRBMS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590026
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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