A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217885



Internal ID22363409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49922890..49922949hg38UCSC Ensembl
chr22:50316538..50316597hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5812n152
Supporting Variantsnssv14304232, nssv14304231
SamplesNA19239, NA19240
Known GenesCRELD2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217885
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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