A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596337



Internal ID16037060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183098699..183099696hg38UCSC Ensembl
Innerchr4:184019852..184020849hg19UCSC Ensembl
Innerchr4:184256846..184257843hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38998
hg19998
hg18998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9416n54
Supporting Variantsnssv1017842
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)nsv596337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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