A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224516



Internal ID20791556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12274078..12275315hg38UCSC Ensembl
chr12:12427012..12428249hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590706
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224516
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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