A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221025



Internal ID20788065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61223964..61225841hg38UCSC Ensembl
chr10:62983722..62985599hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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