A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237462



Internal ID20804502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67242589..67246507hg38UCSC Ensembl
chr14:67709306..67713224hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg383919
hg193919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576233
Supporting Variants
Samples
Known GenesMPP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237462
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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