A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560999



Internal ID20934070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21385456..21386079hg38UCSC Ensembl
chr6:21385687..21386310hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270194
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560999
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