A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278505



Internal ID20845545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66816866..66817448hg38UCSC Ensembl
chr8:67729101..67729683hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573861
Supporting Variants
Samples
Known GenesC8orf44-SGK3, SGK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278505
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00037


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