A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217656



Internal ID20784696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128623804..128626425hg38UCSC Ensembl
chr12:129108349..129110970hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg382622
hg192622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576172
Supporting Variants
Samples
Known GenesTMEM132C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217656
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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