A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482449



Internal ID259907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67784939..67795564hg38UCSC Ensembl
chr10:69544697..69555322hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3810626
hg1910626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482449
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