A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221379



Internal ID20788419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31089902..31091597hg38UCSC Ensembl
chr10:31378831..31380526hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg381696
hg191696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221379
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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