A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551497



Internal ID20924631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6414376..6491856hg38UCSC Ensembl
chr3:6456063..6533543hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3877481
hg1977481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551497
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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