A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236720



Internal ID20803760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104535919..104539998hg38UCSC Ensembl
chr12:104929697..104933776hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg384080
hg194080
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587518
Supporting Variants
Samples
Known GenesCHST11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236720
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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