A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523660



Internal ID299885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12777034..12777616hg38UCSC Ensembl
chr18:12777033..12777615hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17716330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523660
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