A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594100



Internal ID20967171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19080079..19083558hg38UCSC Ensembl
chr16:19091401..19094880hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg383480
hg193480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239173
Samples
Known GenesCOQ7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594100
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