A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18258071



Internal ID20825111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47946379..47965952hg38UCSC Ensembl
chr2:48173518..48193091hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3819574
hg1919574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18258071
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