A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276272



Internal ID20843313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13079665..13080032hg38UCSC Ensembl
chr8:12937174..12937541hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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