A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642563



Internal ID21834610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17754083..17754238hg38UCSC Ensembl
chr22:18236849..18237004hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043868
Supporting Variants
Samples
Known GenesBID
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642563
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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