A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588196



Internal ID20961267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93217246..93217981hg38UCSC Ensembl
chr14:93683592..93684327hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238356
Samples
Known GenesUBR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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