A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551322



Internal ID20924459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35328836..35330108hg38UCSC Ensembl
chr22:35724829..35726101hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381273
hg191273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074182
Samples
Known GenesTOM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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