A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501731



Internal ID278622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15445858..15448030hg38UCSC Ensembl
chr11:15467404..15469576hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382173
hg192173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17041467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501731
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