A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479769



Internal ID257286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89253315..89255301hg38UCSC Ensembl
chr10:91013072..91015058hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg381987
hg191987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479769
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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