A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359521



Internal ID22585190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120940802..120944703hg38UCSC Ensembl
chr11:120811511..120815412hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923783
Supporting Variants
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359521
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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