A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541899



Internal ID20915167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37185680..37185949hg38UCSC Ensembl
chr3:37227171..37227440hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541899
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