A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584324



Internal ID20957395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53172500..53173834hg38UCSC Ensembl
chr14:53639218..53640552hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg381335
hg191335
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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