A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219803



Internal ID20786843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33566858..33568223hg38UCSC Ensembl
chr10:33855786..33857151hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584589
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219803
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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