A curated catalogue of human genomic structural variation




Variant Details

Variant: esv29958



Internal ID11394167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32510376..32554152hg38UCSC Ensembl
Innerchr6:32478153..32521929hg19UCSC Ensembl
Innerchr6:32586131..32629907hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3843777
hg1943777
hg1843777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv84197
SamplesWATSON
Known GenesHLA-DRB5, HLA-DRB6
MethodOligo aCGH
AnalysisThe data were analyzed using the CGH Analytics software.
PlatformAgilent-014584 Human Genome 244K CGH Microarray (Alpha Test)
Comments
ReferenceWheeler_et_al_2008
Pubmed ID18421352
Accession Number(s)esv29958
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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