A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043151



Internal ID96474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5293806..5293899hg38UCSC Ensembl
chr11:5315036..5315129hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043151
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00626


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