A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649238



Internal ID21841285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36044091..36084546hg38UCSC Ensembl
chr22:36440139..36480594hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3840456
hg1940456
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6044924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649238
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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