A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581365



Internal ID20954436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35322432..35323170hg38UCSC Ensembl
chr14:35791638..35792376hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38739
hg19739
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581365
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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