A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568682



Internal ID20941753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85226325..85583279hg38UCSC Ensembl
chr8:86138554..86495508hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38356955
hg19356955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278904
Samples
Known GenesCA1, CA13, CA2, CA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568682
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