A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589933



Internal ID16377342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21990843..22034645hg38UCSC Ensembl
Innerchr3:22032335..22076137hg19UCSC Ensembl
Innerchr3:22007339..22051141hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3843803
hg1943803
hg1843803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960097
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589933
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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