A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17043584



Internal ID96783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2170798..2178040hg38UCSC Ensembl
chr11:2192028..2199270hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387243
hg197243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510762
Supporting Variants
Samples
Known GenesMIR4686, TH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17043584
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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