A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594737



Internal ID16382146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79677642..79748793hg38UCSC Ensembl
Innerchr4:80598796..80669947hg19UCSC Ensembl
Innerchr4:80817820..80888971hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3871152
hg1971152
hg1871152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9143n54
Supporting Variantsnssv1002601
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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