A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5548556



Internal ID322297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31658979..31660859hg38UCSC Ensembl
chr22:32054965..32056845hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728507
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5548556
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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