A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277823



Internal ID20844863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34651465..34652875hg38UCSC Ensembl
chr8:34508983..34510393hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563770
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277823
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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