A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590610



Internal ID16031333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71753901..71754823hg38UCSC Ensembl
Innerchr3:71803052..71803974hg19UCSC Ensembl
Innerchr3:71885742..71886664hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38923
hg19923
hg18923
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965554, nssv965555
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590610
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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