A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223853



Internal ID20790893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76221550..76223218hg38UCSC Ensembl
chr12:76615330..76616998hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg381669
hg191669
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223853
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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