A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594480



Internal ID16381889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:65706139..65763010hg38UCSC Ensembl
Innerchr4:66571857..66628728hg19UCSC Ensembl
Innerchr4:66254452..66311323hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3856872
hg1956872
hg1856872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1001745
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594480
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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