A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589313



Internal ID20962384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:31485168..31485557hg38UCSC Ensembl
chr14:31954374..31954763hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229293
Samples
Known GenesGPR33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589313
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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