A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591367



Internal ID16378776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632551..119634994hg38UCSC Ensembl
Innerchr3:119351398..119353841hg19UCSC Ensembl
Innerchr3:120834088..120836531hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382444
hg192444
hg182444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8519n54
Supporting Variantsnssv971670, nssv971668, nssv971669
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591367
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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