A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356768



Internal ID22582437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13331501..13334148hg38UCSC Ensembl
chr11:13353048..13355695hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382648
hg192648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915617
Supporting Variants
Samples
Known GenesARNTL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356768
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