A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16935131



Internal ID24146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86128020..86139590hg38UCSC Ensembl
chr3:86177170..86188740hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3811571
hg1911571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16935131
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