A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239926



Internal ID20806966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14155096..14155414hg38UCSC Ensembl
chr16:14248953..14249271hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594073
Supporting Variants
Samples
Known GenesMKL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239926
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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