A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568513



Internal ID20941584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108753988..108754988hg38UCSC Ensembl
chr6:109075191..109076191hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267798
Samples
Known GenesLINC00222
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568513
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