A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578542



Internal ID20951613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54924351..54925255hg38UCSC Ensembl
chr14:55391069..55391973hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578542
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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