A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277706



Internal ID20844746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30676384..30677781hg38UCSC Ensembl
chr8:30533901..30535298hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381398
hg191398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567661
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277706
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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