A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569966



Internal ID20943037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83021597..83022195hg38UCSC Ensembl
chr6:83731316..83731914hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38599
hg19599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274779
Samples
Known GenesUBE3D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569966
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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