A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1693n54



Internal ID22769588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22991885..23022607hg38UCSC Ensembl
chr11:23013431..23044153hg19UCSC Ensembl
chr11:22970007..23000729hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3830723
hg1930723
hg1830723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553750, nsv553749
SamplesHGDP00723
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1693n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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