A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588385



Internal ID20961456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22906815..22909079hg38UCSC Ensembl
chr14:23376024..23378288hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382265
hg192265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233083
Samples
Known GenesRBM23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588385
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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