A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613815



Internal ID21805862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120518682..120523992hg38UCSC Ensembl
chr11:120389391..120394701hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385311
hg195311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036985
Supporting Variants
Samples
Known GenesGRIK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613815
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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