A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237392



Internal ID20804432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64519401..64519516hg38UCSC Ensembl
chr14:64986119..64986234hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582792
Supporting Variants
Samples
Known GenesZBTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237392
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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