A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491768



Internal ID268998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71835716..71837204hg38UCSC Ensembl
chr8:72747951..72749439hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg381489
hg191489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491768
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