A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9426n54



Internal ID20142850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186008072..186210350hg38UCSC Ensembl
chr4:186929226..187131504hg19UCSC Ensembl
chr4:187166220..187368498hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38202279
hg19202279
hg18202279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596389, nsv596390, nsv596391
SamplesHGDP00191, HGDP00066, HGDP00264
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)dgv9426n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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