A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279172



Internal ID20846212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96376641..96378191hg38UCSC Ensembl
chr8:97388869..97390419hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381551
hg191551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279172
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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