A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590601



Internal ID16378010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71719619..71726774hg38UCSC Ensembl
Innerchr3:71768770..71775925hg19UCSC Ensembl
Innerchr3:71851460..71858615hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg387156
hg197156
hg187156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965543
Samples
Known GenesEIF4E3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590601
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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