A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569044



Internal ID20942115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143045961..143046327hg38UCSC Ensembl
chr8:144127378..144127744hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277299
Samples
Known GenesC8orf31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569044
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