A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226575



Internal ID20793615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65078294..65079034hg38UCSC Ensembl
chr12:65472074..65472814hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580205
Supporting Variants
Samples
Known GenesWIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226575
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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