A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220282



Internal ID20787322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8705241..8706447hg38UCSC Ensembl
chr12:8857837..8859043hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582474
Supporting Variants
Samples
Known GenesRIMKLB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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