A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230690



Internal ID20797730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32888627..32890022hg38UCSC Ensembl
chr12:33041561..33042956hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381396
hg191396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594871
Supporting Variants
Samples
Known GenesPKP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230690
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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