A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590550



Internal ID16031273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66384219..66457018hg38UCSC Ensembl
Innerchr3:66434643..66507442hg19UCSC Ensembl
Innerchr3:66517333..66590132hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3872800
hg1972800
hg1872800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv964211
Samples
Known GenesLRIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590550
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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