A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5341n54



Internal ID20138765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907804..89908560hg38UCSC Ensembl
chr16:89974212..89974968hg19UCSC Ensembl
chr16:88501713..88502469hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573837, nsv573838, nsv573840
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5341n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss9
Observed Complex0
Frequencyn/a


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