A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594919



Internal ID16382328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96706588..96767158hg38UCSC Ensembl
Innerchr4:97627739..97688309hg19UCSC Ensembl
Innerchr4:97846762..97907332hg18UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3860571
hg1960571
hg1860571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1003389
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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