A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293264



Internal ID20502482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1894042..1939760hg38UCSC Ensembl
chr11:1915272..1960990hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3845719
hg1945719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757623
Supporting Variants
Samples
Known GenesTNNT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293264
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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