A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6842n71



Internal ID6324462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43536401..43554535hg19UCSC Ensembl
chr6:43644379..43662513hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv885847, nsv885846
SamplesSP54956, SP57469, SP56223, SP55021
Known GenesPOLH, XPO5
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6842n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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