A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596391



Internal ID16037114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186010756..186210350hg38UCSC Ensembl
Innerchr4:186931910..187131504hg19UCSC Ensembl
Innerchr4:187168904..187368498hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38199595
hg19199595
hg18199595
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9426n54
Supporting Variantsnssv1152987
SamplesHGDP00264
Known GenesCYP4V2, FAM149A, FLJ38576, TLR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596391
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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