A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564692



Internal ID20937763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33481255..33481950hg38UCSC Ensembl
chr8:33338773..33339468hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564692
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