A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1919e1



Internal ID6309717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31028290..31352778hg19UCSC Ensembl
chr6:31136269..31460757hg18UCSC Ensembl
chr6:31136269..31460757hg17UCSC 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 Variantsessv22195, essv20068, essv16474, essv21076, essv21839, essv23868
SamplesNA12044, NA11839, NA12814, NA07048, NA19139, NA06991
Known GenesC6orf15, CCHCR1, CDSN, HCG27, HLA-B, HLA-C, POU5F1, PSORS1C1, PSORS1C2, PSORS1C3, TCF19
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv1919e1
Frequency
Sample Size271
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer