A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219012



Internal ID20786052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110065359..110066271hg38UCSC Ensembl
chr12:110503164..110504076hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580308
Supporting Variants
Samples
Known GenesC12orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219012
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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