A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235029



Internal ID20802069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21493866..21494586hg38UCSC Ensembl
chr14:21962025..21962745hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581534
Supporting Variants
Samples
Known GenesTOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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