A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049678



Internal ID101012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86589089..86590672hg38UCSC Ensembl
chr11:86300131..86301714hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381584
hg191584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501671
Supporting Variants
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049678
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