A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734222



Internal ID157888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19035679..19037436hg38UCSC Ensembl
chr21:20407998..20409755hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381758
hg191758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734222
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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