A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222399



Internal ID20789439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106313555..106314025hg38UCSC Ensembl
chr12:106707333..106707803hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585019
Supporting Variants
Samples
Known GenesTCP11L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222399
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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