A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505296



Internal ID282078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120103768..120107373hg38UCSC Ensembl
chr10:121863280..121866885hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg383606
hg193606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505296
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