A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232859



Internal ID20799900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122344627..122348191hg38UCSC Ensembl
chr10:124104142..124107706hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383565
hg193565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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