A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584964



Internal ID16372373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241567093..241567855hg38UCSC Ensembl
Innerchr2:242506508..242507270hg19UCSC Ensembl
Innerchr2:242155181..242155943hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38763
hg19763
hg18763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7392n54
Supporting Variantsnssv934724
Samples
Known GenesBOK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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