A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103580



Internal ID21270818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:45158685..45160665hg38UCSC Ensembl
Innerchr22:45554566..45556546hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381981
hg191981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110734
Supporting Variants
Samplessample155
Known GenesLOC100506714
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103580
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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