A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478835



Internal ID256381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135210692..135210770hg38UCSC Ensembl
chr7:134895444..134895522hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17003677
Samples
Known GenesWDR91
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478835
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