A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268481



Internal ID20835521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111181054..111182019hg38UCSC Ensembl
chr6:111502257..111503222hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38966
hg19966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563338
Supporting Variants
Samples
Known GenesSLC16A10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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