A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584882



Internal ID16372291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240869364..240878099hg38UCSC Ensembl
Innerchr2:241808781..241817516hg19UCSC Ensembl
Innerchr2:241457454..241466189hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg388736
hg198736
hg188736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7374n54
Supporting Variantsnssv934084
Samples
Known GenesAGXT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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