A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567111



Internal ID20940182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179517489..179525740hg38UCSC Ensembl
chr3:179235277..179243528hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg388252
hg198252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567111
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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