A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4464n223



Internal ID22807432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:42540129..42621071hg38UCSC Ensembl
chr20:41168769..41249711hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3880943
hg1980943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6540665, nsv6555414
Samples
Known GenesPTPRT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4464n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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