A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589938



Internal ID16377347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22189652..22330962hg38UCSC Ensembl
Innerchr3:22231144..22372453hg19UCSC Ensembl
Innerchr3:22206148..22347457hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38141311
hg19141310
hg18141310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960100
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589938
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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