A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2070e1



Internal ID6309868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22755584..22920910hg19UCSC Ensembl
chr7:22722109..22887435hg18UCSC Ensembl
chr7:22528824..22694150hg17UCSC Ensembl
Cytoband7p15.3
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 Variantsesv185, essv23565
SamplesNA06993
Known GenesIL6, SNORD93, TOMM7
Method
Analysis
Platform
Comments
ReferenceRedon et al 2006
Pubmed ID17122850
Accession Number(s)dgv2070e1
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