A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584861



Internal ID20957932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98813856..98819869hg38UCSC Ensembl
chr14:99280193..99286206hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg386014
hg196014
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584861
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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