A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592760



Internal ID16380169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188752450..188848518hg38UCSC Ensembl
Innerchr3:188470238..188566306hg19UCSC Ensembl
Innerchr3:189952932..190049000hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3896069
hg1996069
hg1896069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982902
Samples
Known GenesLPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592760
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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