A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585050



Internal ID16372459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241931649..242085907hg38UCSC Ensembl
Innerchr2:242873800..243028058hg19UCSC Ensembl
Innerchr2:242522473..242676731hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38154259
hg19154259
hg18154259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7399n54
Supporting Variantsnssv934909
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585050
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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