A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256362



Internal ID20823402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200927396..200928059hg38UCSC Ensembl
chr2:201792119..201792782hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546318
Supporting Variants
Samples
Known GenesORC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256362
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00048


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