A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474868



Internal ID252518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72675494..72681358hg38UCSC Ensembl
chr10:74435252..74441116hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg385865
hg195865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474868
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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