A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590600



Internal ID16031323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71717301..71780868hg38UCSC Ensembl
Innerchr3:71766452..71830019hg19UCSC Ensembl
Innerchr3:71849142..71912709hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3863568
hg1963568
hg1863568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965542
Samples
Known GenesEIF4E3, GPR27, PROK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590600
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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