A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589990



Internal ID21782033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8099782..8099782hg38UCSC Ensembl
chr11:8121329..8121329hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385934
hg195934
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6099703
Supporting Variants
Samples
Known GenesTUB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589990
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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