A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593258



Internal ID20966329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23032015..23032773hg38UCSC Ensembl
chr14:23501224..23501982hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218233
Samples
Known GenesPSMB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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