A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593639



Internal ID16034362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:8392649..8422381hg38UCSC Ensembl
Innerchr4:8394376..8424108hg19UCSC Ensembl
Innerchr4:8445276..8475008hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3829733
hg1929733
hg1829733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv991249
Samples
Known GenesACOX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593639
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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