A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596052



Internal ID16383461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165533674..165567463hg38UCSC Ensembl
Innerchr4:166454826..166488615hg19UCSC Ensembl
Innerchr4:166674276..166708065hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3833790
hg1933790
hg1833790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1012557
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596052
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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