A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731658



Internal ID155324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23974827..23981165hg38UCSC Ensembl
chr20:23955464..23961802hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg386339
hg196339
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731658
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.006869


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