A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594388



Internal ID16381797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63272623..63427426hg38UCSC Ensembl
Innerchr4:64138341..64293144hg19UCSC Ensembl
Innerchr4:63820936..63975739hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38154804
hg19154804
hg18154804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1000710
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594388
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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