A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584792



Internal ID16372201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:239400751..239401967hg38UCSC Ensembl
Innerchr2:240322445..240323661hg19UCSC Ensembl
Innerchr2:239987382..239988598hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381217
hg191217
hg181217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7357n54
Supporting Variantsnssv933815
Samples
Known GenesHDAC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584792
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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