A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235748



Internal ID20802788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98527225..98528566hg38UCSC Ensembl
chr12:98921003..98922344hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381342
hg191342
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586444
Supporting Variants
Samples
Known GenesTMPO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235748
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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