A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596338



Internal ID16383747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183098699..183099765hg38UCSC Ensembl
Innerchr4:184019852..184020918hg19UCSC Ensembl
Innerchr4:184256846..184257912hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381067
hg191067
hg181067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9416n54
Supporting Variantsnssv1017843
Samples
Known GenesWWC2, WWC2-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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