A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490399



Internal ID267656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61992388..61998001hg38UCSC Ensembl
chr8:62904947..62910560hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg385614
hg195614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv509n206
Supporting Variantsnssv17011730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490399
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