A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560344



Internal ID20933415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142708261..142709721hg38UCSC Ensembl
chr3:142427103..142428563hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262485
Samples
Known GenesPLS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560344
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