A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583588



Internal ID16370997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:166701394..166733235hg38UCSC Ensembl
Innerchr2:167557904..167589745hg19UCSC Ensembl
Innerchr2:167266150..167297991hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3831842
hg1931842
hg1831842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv925266
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583588
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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