A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463058



Internal ID240974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1107979..1108351hg38UCSC Ensembl
chr7:1147615..1147987hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991732
Samples
Known GenesC7orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463058
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