A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591369



Internal ID16378778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:119632551..119635046hg38UCSC Ensembl
Innerchr3:119351398..119353893hg19UCSC Ensembl
Innerchr3:120834088..120836583hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg382496
hg192496
hg182496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8519n54
Supporting Variantsnssv971673, nssv971672
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591369
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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