A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541317



Internal ID315937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44502672..44503367hg38UCSC Ensembl
chr22:44898552..44899247hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541317
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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