A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360509



Internal ID22586178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58832259..58997961hg38UCSC Ensembl
chr11:58599732..58765434hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38165703
hg19165703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918762
Supporting Variants
Samples
Known GenesGLYATL1, GLYATL2, LOC283194
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360509
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