A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278571



Internal ID20845611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68949674..68951985hg38UCSC Ensembl
chr8:69861909..69864220hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382312
hg192312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572531
Supporting Variants
Samples
Known GenesLOC100505718
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278571
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer