A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1918e1



Internal ID6309716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31028290..31234581hg19UCSC Ensembl
chr6:31136269..31342560hg18UCSC Ensembl
chr6:31136269..31342560hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Complex
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv12313, essv22306, essv10053, essv19239, essv21551, essv18965
SamplesNA12005, NA12873, NA06985, NA19138, NA19099, NA10838
Known GenesC6orf15, CCHCR1, CDSN, HCG27, POU5F1, PSORS1C1, PSORS1C2, PSORS1C3, TCF19
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv1918e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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