A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236864



Internal ID20803904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49997240..49998050hg38UCSC Ensembl
chr14:50463958..50464768hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38811
hg19811
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589315
Supporting Variants
Samples
Known GenesC14orf182
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00016


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