A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526226



Internal ID302364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50149735..50149795hg38UCSC Ensembl
chr20:48766272..48766332hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732869
Samples
Known GenesTMEM189, TMEM189-UBE2V1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526226
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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