A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5139n54



Internal ID20138563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57092192..57093081hg38UCSC Ensembl
chr16:57126104..57126993hg19UCSC Ensembl
chr16:55683605..55684494hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38890
hg19890
hg18890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572708, nsv572698, nsv572709
Samples
Known GenesCPNE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5139n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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