A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921401



Internal ID22696625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18076345..18078565hg38UCSC Ensembl
chr11:18097892..18100112hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382221
hg192221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921401
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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