A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220034



Internal ID20787074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18276631..18277074hg38UCSC Ensembl
chr10:18565560..18566003hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576805
Supporting Variants
Samples
Known GenesCACNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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