A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271045



Internal ID20480263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48616906..48616972hg38UCSC Ensembl
chr16:48650817..48650883hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756786
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271045
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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