A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275886



Internal ID20842926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100250816..100250923hg38UCSC Ensembl
chr8:101263044..101263151hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275886
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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