A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731680



Internal ID155346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24390207..24406513hg38UCSC Ensembl
chr20:24370843..24387149hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3816307
hg1916307
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560508
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731680
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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