A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236293



Internal ID20803333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113077570..113172440hg38UCSC Ensembl
chr12:113515375..113610245hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3894871
hg1994871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581180
Supporting Variants
Samples
Known GenesCCDC42B, DDX54, DTX1, MIR7106, RASAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236293
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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