A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256412



Internal ID20823452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202215930..202216901hg38UCSC Ensembl
chr2:203080653..203081624hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545866
Supporting Variants
Samples
Known GenesSUMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256412
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