A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590121



Internal ID16377530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41318043..41780279hg38UCSC Ensembl
Innerchr3:41359534..41821771hg19UCSC Ensembl
Innerchr3:41334538..41796775hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38462237
hg19462238
hg18462238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8290n54
Supporting Variantsnssv962398
Samples
Known GenesULK4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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