A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501211



Internal ID278116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58912942..58913495hg38UCSC Ensembl
chr13:59487076..59487629hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501211
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