A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258787



Internal ID20825827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64924875..64926730hg38UCSC Ensembl
chr2:65152009..65153864hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381856
hg191856
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553456
Supporting Variants
Samples
Known GenesLOC400958
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258787
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