A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218007



Internal ID20785047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110211869..110212240hg38UCSC Ensembl
chr12:110649674..110650045hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587727
Supporting Variants
Samples
Known GenesIFT81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218007
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer