A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584115



Internal ID16371524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:195049982..195219659hg38UCSC Ensembl
Innerchr2:195914706..196084383hg19UCSC Ensembl
Innerchr2:195622951..195792628hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38169678
hg19169678
hg18169678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv930184
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584115
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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