A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910887



Internal ID8022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20068849..20069527hg38UCSC Ensembl
chr2:20268610..20269288hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910887
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