A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517431



Internal ID293853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32305234..32306946hg38UCSC Ensembl
chr20:30893037..30894749hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381713
hg191713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731946
Samples
Known GenesKIF3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517431
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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