A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593466



Internal ID16034189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3751690..3765829hg38UCSC Ensembl
Innerchr4:3753417..3767556hg19UCSC Ensembl
Innerchr4:3723215..3737354hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3814140
hg1914140
hg1814140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8928n54
Supporting Variantsnssv989295
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593466
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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