A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573687



Internal ID20946758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108564459..108570325hg38UCSC Ensembl
chr3:108283306..108289172hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg385867
hg195867
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259137
Samples
Known GenesKIAA1524
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573687
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