A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591314



Internal ID20964385
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 StatusM
Merged Variants
Supporting Variantsnssv18238212
Samples
Known GenesSEL1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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