A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260614



Internal ID20827654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39495705..39496971hg38UCSC Ensembl
chr3:39537196..39538462hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548669
Supporting Variants
Samples
Known GenesMOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260614
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