A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224539



Internal ID20791579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111939776..111940256hg38UCSC Ensembl
chr12:112377580..112378060hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590634
Supporting Variants
Samples
Known GenesTMEM116
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224539
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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