A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540882



Internal ID20914170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42608212..42609024hg38UCSC Ensembl
chr3:42649704..42650516hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260681
Samples
Known GenesNKTR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540882
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