A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047096



Internal ID99237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60073255..60073306hg38UCSC Ensembl
chr11:59840728..59840779hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5513653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer