A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592758



Internal ID16380167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188356989..188526821hg38UCSC Ensembl
Innerchr3:188074777..188244609hg19UCSC Ensembl
Innerchr3:189557471..189727303hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38169833
hg19169833
hg18169833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv982901
Samples
Known GenesLPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592758
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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