A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192646



Internal ID20759686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122660937..122819103hg38UCSC Ensembl
chr11:122531645..122689811hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38158167
hg19158167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473894
Supporting Variants
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192646
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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