A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5280n54



Internal ID22773175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86205475..86226996hg38UCSC Ensembl
chr16:86239081..86260602hg19UCSC Ensembl
chr16:84796582..84818103hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3821522
hg1921522
hg1821522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573524, nsv573523
Samples
Known GenesLINC01081
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5280n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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