A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557367



Internal ID330466
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 StatusM
Merged Variants
Supporting Variantsnssv17731658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557367
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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