A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477878



Internal ID255444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108451308..108451674hg38UCSC Ensembl
chr8:109463537..109463903hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015126
Samples
Known GenesEMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477878
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