A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237450



Internal ID20804490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67009992..67010350hg38UCSC Ensembl
chr14:67476709..67477067hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580277
Supporting Variants
Samples
Known GenesGPHN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237450
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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