A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277434



Internal ID20844474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19754429..19790383hg38UCSC Ensembl
chr8:19611940..19647894hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3835955
hg1935955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573823
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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