A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596357



Internal ID16383766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184825411..184826321hg38UCSC Ensembl
Innerchr4:185746565..185747475hg19UCSC Ensembl
Innerchr4:185983559..185984469hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38911
hg19911
hg18911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9419n54
Supporting Variantsnssv1017963
Samples
Known GenesACSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596357
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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