A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271993



Internal ID20839033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46656397..46657148hg38UCSC Ensembl
chr6:46624134..46624885hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570411
Supporting Variants
Samples
Known GenesSLC25A27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271993
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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