A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578876



Internal ID20951947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89882243..89919001hg38UCSC Ensembl
chr14:90348587..90385345hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3836759
hg1936759
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237634
Samples
Known GenesEFCAB11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578876
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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