A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726023



Internal ID149689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47904922..48493763hg38UCSC Ensembl
chr20:46533666..47122009hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38588842
hg19588344
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558385
Supporting Variants
Samples
Known GenesLINC00494
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726023
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.007181


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