A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292841



Internal ID20502059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120516918..120517649hg38UCSC Ensembl
chr11:120387627..120388358hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735741
Supporting Variants
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292841
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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