A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223279



Internal ID20790319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9323112..9406544hg38UCSC Ensembl
chr12:9475708..9559140hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3883433
hg1983433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584510
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223279
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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