A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592763



Internal ID16380172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189405644..189441563hg38UCSC Ensembl
Innerchr3:189123433..189159352hg19UCSC Ensembl
Innerchr3:190606127..190642046hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3835920
hg1935920
hg1835920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982905
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592763
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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