A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226388



Internal ID20793428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96066298..96067681hg38UCSC Ensembl
chr12:96460076..96461459hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381384
hg191384
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226388
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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