A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593971



Internal ID20967042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34820236..34822025hg38UCSC Ensembl
chr14:35289442..35291231hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg381790
hg191790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219200
Samples
Known GenesBAZ1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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