A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1639n54



Internal ID22769534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8178669..8194306hg38UCSC Ensembl
chr11:8200216..8215853hg19UCSC Ensembl
chr11:8156792..8172429hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3815638
hg1915638
hg1815638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553443, nsv553445, nsv553444
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1639n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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