A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728993



Internal ID152659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39203466..39293496hg38UCSC Ensembl
chr22:39599471..39689501hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3890031
hg1990031
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558127
Supporting Variants
Samples
Known GenesPDGFB
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728993
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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