A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552950



Internal ID20926068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41086844..41089650hg38UCSC Ensembl
chr22:41482848..41485654hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg382807
hg192807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552950
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