A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596388



Internal ID16383797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185963182..186014681hg38UCSC Ensembl
Innerchr4:186884336..186935835hg19UCSC Ensembl
Innerchr4:187121330..187172829hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3851500
hg1951500
hg1851500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1019560
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596388
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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