A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496276



Internal ID273354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65414632..65425044hg38UCSC Ensembl
chr11:65182103..65192515hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3810413
hg1910413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045214
Samples
Known GenesNEAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496276
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