A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047678



Internal ID99656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69138047..69139015hg38UCSC Ensembl
chr11:68905515..68906483hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047678
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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