A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277295



Internal ID20844335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142966653..142967255hg38UCSC Ensembl
chr8:144048070..144048672hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558159
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277295
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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