A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535078



Internal ID310790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35064783..35171588hg38UCSC Ensembl
chr22:35460776..35567581hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38106806
hg19106806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728688
Samples
Known GenesISX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535078
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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