A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220012



Internal ID20787052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24833529..24833795hg38UCSC Ensembl
chr12:24986463..24986729hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585188
Supporting Variants
Samples
Known GenesBCAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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