A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228853



Internal ID20795893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31393268..31393861hg38UCSC Ensembl
chr14:31862474..31863067hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592740
Supporting Variants
Samples
Known GenesHEATR5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228853
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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