A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1698n54



Internal ID22769593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23980429..24070136hg38UCSC Ensembl
chr11:24001975..24091682hg19UCSC Ensembl
chr11:23958551..24048258hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3889708
hg1989708
hg1889708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553773, nsv553776
Samples1780862432_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1698n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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