A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277400



Internal ID20844440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18075013..18524799hg38UCSC Ensembl
chr8:17932522..18382309hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38449787
hg19449788
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563587
Supporting Variants
Samples
Known GenesASAH1, NAT1, NAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277400
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