A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042851



Internal ID96273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11814540..11821322hg38UCSC Ensembl
chr11:11836087..11842869hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg386783
hg196783
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555200
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042851
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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