A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234904



Internal ID20801944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132363629..132411062hg38UCSC Ensembl
chr12:132940215..132987648hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3847434
hg1947434
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578170
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234904
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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