A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236382



Internal ID20803422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:129333276..129334288hg38UCSC Ensembl
chr12:129817821..129818833hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381013
hg191013
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578896
Supporting Variants
Samples
Known GenesTMEM132D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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