A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256383



Internal ID20823423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201217565..201217780hg38UCSC Ensembl
chr2:202082288..202082503hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547247
Supporting Variants
Samples
Known GenesCASP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256383
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