A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041707



Internal ID95511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6688292..6688343hg38UCSC Ensembl
chr11:6709523..6709574hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381290
hg191290
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041707
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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