A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541081



Internal ID20914367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41310806..41311671hg38UCSC Ensembl
chr3:41352297..41353162hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260634
Samples
Known GenesULK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541081
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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