A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9158n54



Internal ID22777053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89651171..89709750hg38UCSC Ensembl
chr4:90572322..90630901hg19UCSC Ensembl
chr4:90791345..90849924hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3858580
hg1958580
hg1858580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594818, nsv594819
SamplesHGDP00392, HGDP00351, HGDP00359
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9158n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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