A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541763



Internal ID316321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24860897..24861352hg38UCSC Ensembl
chr22:25256864..25257319hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38456
hg19456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728106
Samples
Known GenesSGSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541763
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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