A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501671



Internal ID278564
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 StatusM
Merged Variants
Supporting Variantsnssv17049678
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501671
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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