A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220732



Internal ID20787772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21466408..21466992hg38UCSC Ensembl
chr10:21755337..21755921hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220732
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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