A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590603



Internal ID16031326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71725034..71754823hg38UCSC Ensembl
Innerchr3:71774185..71803974hg19UCSC Ensembl
Innerchr3:71856875..71886664hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3829790
hg1929790
hg1829790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8373n54
Supporting Variantsnssv965545, nssv965546
Samples
Known GenesEIF4E3, GPR27
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590603
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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