A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254560



Internal ID20821600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:150078090..150079795hg38UCSC Ensembl
chr2:150934604..150936309hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381706
hg191706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254560
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