A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226593



Internal ID20793633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80393351..80394058hg38UCSC Ensembl
chr10:82153107..82153814hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226593
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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