A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220156



Internal ID20787196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110495010..110495693hg38UCSC Ensembl
chr12:110932815..110933498hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583430
Supporting Variants
Samples
Known GenesVPS29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220156
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