A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275720



Internal ID20484938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46384671..46396548hg38UCSC Ensembl
chr16:46418583..46430460hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3811878
hg1911878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762591
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275720
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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