A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231747



Internal ID20798787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20450832..20451440hg38UCSC Ensembl
chr14:20918991..20919599hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589645
Supporting Variants
Samples
Known GenesOSGEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231747
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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