A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276262



Internal ID20843303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130215034..130215888hg38UCSC Ensembl
chr8:131227280..131228134hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566435
Supporting Variants
Samples
Known GenesASAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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