A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578861



Internal ID20951932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9550888..9553033hg38UCSC Ensembl
chr16:9644745..9646890hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg382146
hg192146
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578861
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