A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436237



Internal ID214857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101595712..101595994hg38UCSC Ensembl
chr3:101314556..101314838hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436237
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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