A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592762



Internal ID16380171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188769242..188815021hg38UCSC Ensembl
Innerchr3:188487030..188532809hg19UCSC Ensembl
Innerchr3:189969724..190015503hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3845780
hg1945780
hg1845780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8778n54
Supporting Variantsnssv982904
Samples
Known GenesLPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592762
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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