A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575282



Internal ID20948353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132991387..132992265hg38UCSC Ensembl
chr8:134003632..134004510hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7499n223
Supporting Variantsnssv18277151
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575282
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