A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727356



Internal ID151023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10834643..10853100hg38UCSC Ensembl
chrUn_gl000244:1..18457hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3818458
hg1918457
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727356
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.186188


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