A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578616



Internal ID20951687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:68848549..68849178hg38UCSC Ensembl
chr14:69315266..69315895hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578616
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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