A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2191n223



Internal ID22805159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70957380..71221475hg38UCSC Ensembl
chr14:71424097..71688192hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38264096
hg19264096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6476858, nsv6479069
Samples
Known GenesPCNX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2191n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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