A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18238212



Internal ID20805253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81480221..81480707hg38UCSC Ensembl
chr14:81946565..81947051hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591314
Supporting Variants
Samples
Known GenesSEL1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18238212
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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