A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584991



Internal ID16025714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241805306..242006956hg38UCSC Ensembl
Innerchr2:242744983..242949107hg19UCSC Ensembl
Innerchr2:242393656..242597780hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38201651
hg19204125
hg18204125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv934812
Samples
Known GenesCXXC11, NEU4, PDCD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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