A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561196



Internal ID20934267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142159267..142159848hg38UCSC Ensembl
chr6:142480404..142480985hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272552
Samples
Known GenesVTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561196
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