A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728960



Internal ID152626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38806272..38808556hg38UCSC Ensembl
chr22:39202277..39204561hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg382285
hg192285
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728960
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.496128


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer