A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227107



Internal ID20794147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100042113..100042816hg38UCSC Ensembl
chr10:101801870..101802573hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588003
Supporting Variants
Samples
Known GenesCPN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227107
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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