A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584030



Internal ID16371439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:186050710..186136349hg38UCSC Ensembl
Innerchr2:186915437..187001076hg19UCSC Ensembl
Innerchr2:186623682..186709321hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3885640
hg1985640
hg1885640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv928238
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584030
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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