A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv991n71



Internal ID6318611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1964312..2016908hg19UCSC Ensembl
chr11:1920888..1973484hg18UCSC 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 Variantsnsv896766, nsv896762, nsv896761
SamplesSP54956, SP54657, SP54725
Known GenesH19, MRPL23, MRPL23-AS1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv991n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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