A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6951n71



Internal ID6324571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99274066..99297567hg19UCSC Ensembl
chr6:99380787..99404288hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv886435, nsv886434
SamplesSP54956, SP54725
Known GenesPOU3F2
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv6951n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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