A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225599



Internal ID20792639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125307653..125307812hg38UCSC Ensembl
chr12:125792199..125792358hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225599
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.48113


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