A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936839



Internal ID25277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99027824..99085713hg38UCSC Ensembl
chr3:98746668..98804557hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3857890
hg1957890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440578
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936839
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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