A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594029



Internal ID16381438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39708474..39714520hg38UCSC Ensembl
Innerchr4:39710094..39716140hg19UCSC Ensembl
Innerchr4:39386489..39392535hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg386047
hg196047
hg186047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995977
Samples
Known GenesUBE2K
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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