A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1756n54



Internal ID22769651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38674924..38782664hg38UCSC Ensembl
chr11:38696474..38804214hg19UCSC Ensembl
chr11:38653050..38760790hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38107741
hg19107741
hg18107741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554070, nsv554069
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1756n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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