A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547934



Internal ID20921133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33419618..33420828hg38UCSC Ensembl
chr3:33461110..33462320hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262042
Samples
Known GenesUBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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