A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555975



Internal ID329123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57480178..57491282hg38UCSC Ensembl
chr20:56055234..56066338hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3811105
hg1911105
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555975
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer