A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2046n54



Internal ID22769941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86571638..86575599hg38UCSC Ensembl
chr11:86282680..86286641hg19UCSC Ensembl
chr11:85960328..85964289hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383962
hg193962
hg183962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555670, nsv555666, nsv555668, nsv555667, nsv555669
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2046n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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