A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584794



Internal ID20957865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79159964..79222107hg38UCSC Ensembl
chr14:79626307..79688450hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3862144
hg1962144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238178
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584794
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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