A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594336



Internal ID16381745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62209696..62317528hg38UCSC Ensembl
Innerchr4:63075414..63183246hg19UCSC Ensembl
Innerchr4:62758009..62865841hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38107833
hg19107833
hg18107833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9072n54
Supporting Variantsnssv1000260
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594336
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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