A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223370



Internal ID20790410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92189500..92192968hg38UCSC Ensembl
chr12:92583276..92586744hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg383469
hg193469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223370
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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