A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603890



Internal ID21795937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119358268..119358414hg38UCSC Ensembl
chr11:119228978..119229124hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022151
Supporting Variants
Samples
Known GenesUSP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603890
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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