A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4168n71



Internal ID6321788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75012327..75281054hg19UCSC Ensembl
chr2:74865835..75134562hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv874298, nsv874297
SamplesIS33622, SP81187
Known GenesHK2, POLE4, TACR1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv4168n71
Frequency
Sample Size6533
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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