A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584075



Internal ID16371484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:193277046..193534507hg38UCSC Ensembl
Innerchr2:194141771..194399232hg19UCSC Ensembl
Innerchr2:193850016..194107477hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38257462
hg19257462
hg18257462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv928440
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584075
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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