A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596004



Internal ID16383413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:162362304..162408149hg38UCSC Ensembl
Innerchr4:163283456..163329301hg19UCSC Ensembl
Innerchr4:163502906..163548751hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3845846
hg1945846
hg1845846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9363n54
Supporting Variantsnssv1010533
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596004
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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