A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596146



Internal ID16383555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170287780..170367322hg38UCSC Ensembl
Innerchr4:171208931..171288473hg19UCSC Ensembl
Innerchr4:171445506..171525048hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3879543
hg1979543
hg1879543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1013012, nssv1013011
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596146
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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