A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537840



Internal ID20911172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113788104..113789722hg38UCSC Ensembl
chr2:114545681..114547299hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381619
hg191619
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4086n223
Supporting Variantsnssv18256550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537840
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer