A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582357



Internal ID20955428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79778197..79779151hg38UCSC Ensembl
chr14:80244540..80245494hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238186
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582357
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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