A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502933



Internal ID279781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86820714..86823907hg38UCSC Ensembl
chr11:86531756..86534949hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383194
hg193194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502933
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