A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222173



Internal ID20789213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119639336..119640456hg38UCSC Ensembl
chr12:120077141..120078261hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381121
hg191121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585904
Supporting Variants
Samples
Known GenesTMEM233
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222173
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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