A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480901



Internal ID258398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65920815..65923195hg38UCSC Ensembl
chr7:65385802..65388182hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382381
hg192381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997601
Samples
Known GenesVKORC1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480901
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