A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592029



Internal ID16379438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149551402..149552236hg38UCSC Ensembl
Innerchr3:149269189..149270023hg19UCSC Ensembl
Innerchr3:150751879..150752713hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38835
hg19835
hg18835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8648n54
Supporting Variantsnssv976718, nssv976711, nssv976714, nssv976713, nssv976715, nssv976716, nssv976712, nssv976719, nssv976717
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592029
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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