A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5263n71



Internal ID6322883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138645013..138673922hg19UCSC Ensembl
chr3:140127703..140156612hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv877541, nsv877540
SamplesSP54956, SP54988
Known GenesC3orf72, FOXL2
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv5263n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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