A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5141n54



Internal ID22773036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57092397..57093237hg38UCSC Ensembl
chr16:57126309..57127149hg19UCSC Ensembl
chr16:55683810..55684650hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38841
hg19841
hg18841
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv572715, nsv572717
Samples
Known GenesCPNE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5141n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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