A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593463



Internal ID16380872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3668959..3712458hg38UCSC Ensembl
Innerchr4:3670686..3714185hg19UCSC Ensembl
Innerchr4:3640484..3683983hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3843500
hg1943500
hg1843500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8927n54
Supporting Variantsnssv1152583
SamplesHGDP00546
Known GenesLOC100133461
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593463
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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