A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562494



Internal ID20935565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122850249..122851270hg38UCSC Ensembl
chr8:123862488..123863509hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276101
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562494
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