A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1696n54



Internal ID22769591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23759988..23819629hg38UCSC Ensembl
chr11:23781534..23841175hg19UCSC Ensembl
chr11:23738110..23797751hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3859642
hg1959642
hg1859642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553768, nsv553766, nsv553765
Samples1780862310_A, 1780854341_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1696n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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