A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584109



Internal ID16371518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194488162..194842000hg38UCSC Ensembl
Innerchr2:195352886..195706724hg19UCSC Ensembl
Innerchr2:195061131..195414969hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38353839
hg19353839
hg18353839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151124
SamplesHGDP01338
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584109
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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