A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591926



Internal ID16379335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144155059..144339553hg38UCSC Ensembl
Innerchr3:143873901..144058395hg19UCSC Ensembl
Innerchr3:145356591..145541085hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38184495
hg19184495
hg18184495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8628n54
Supporting Variantsnssv975225
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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