A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258014



Internal ID20825054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45939751..45940925hg38UCSC Ensembl
chr2:46166890..46168064hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381175
hg191175
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547315
Supporting Variants
Samples
Known GenesPRKCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258014
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