A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492647



Internal ID269855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92473622..92476320hg38UCSC Ensembl
chr7:92102936..92105634hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg382699
hg192699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492647
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