A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043291



Internal ID96571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10764901..10764952hg38UCSC Ensembl
chr11:10786448..10786499hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542459
Supporting Variants
Samples
Known GenesCTR9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043291
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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