A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437259



Internal ID215853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96680884..96687891hg38UCSC Ensembl
chr3:96399728..96406735hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg387008
hg197008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv352n206
Supporting Variantsnssv16935172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437259
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