A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1613n54



Internal ID22769508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5739717..5740399hg38UCSC Ensembl
chr11:5760947..5761629hg19UCSC Ensembl
chr11:5717523..5718205hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38683
hg19683
hg18683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553293, nsv553297
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1613n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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