A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543974



Internal ID20917215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65405673..65407212hg38UCSC Ensembl
chr3:65391348..65392887hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381540
hg191540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263954
Samples
Known GenesMAGI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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