A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv988n71



Internal ID6318608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1944202..2029278hg19UCSC Ensembl
chr11:1900778..1985854hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv896756, nsv896763
SamplesIS40502, IS38538
Known GenesH19, MIR675, MRPL23, MRPL23-AS1, TNNT3
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv988n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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