A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728778



Internal ID152444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36453080..36455832hg38UCSC Ensembl
chr22:36849127..36851879hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382753
hg192753
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555544
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728778
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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