A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278337



Internal ID20845377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58494854..58495453hg38UCSC Ensembl
chr8:59407413..59408012hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555700
Supporting Variants
Samples
Known GenesCYP7A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278337
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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