A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218897



Internal ID20785937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98523798..98524292hg38UCSC Ensembl
chr12:98917576..98918070hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585081
Supporting Variants
Samples
Known GenesTMPO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218897
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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