A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7466n71



Internal ID6325086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117129404..117246315hg19UCSC Ensembl
chr7:116916640..117033551hg18UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv889078, nsv889077
SamplesIS31205, IS33533
Known GenesCFTR
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv7466n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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