A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562235



Internal ID335193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72563377..72563377hg38UCSC Ensembl
chr14:73030085..73030085hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696044
Samples
Known GenesRGS6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562235
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