A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455996



Internal ID234065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45646159..45646705hg38UCSC Ensembl
chr6:45613896..45614442hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455996
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