A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv987n71



Internal ID6318607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1917872..2066031hg19UCSC Ensembl
chr11:1874448..2022607hg18UCSC 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 Variantsnsv896755, nsv896750, nsv896751, nsv896752, nsv896753, nsv896754
SamplesIS33684, IS38840, IS39258, MS17208, MS16153, IS32737, MS11306, MS13770
Known GenesH19, MIR675, MRPL23, MRPL23-AS1, TNNT3
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv987n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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