A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572093



Internal ID20945164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132301641..132304530hg38UCSC Ensembl
chr3:132020485..132023374hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382890
hg192890
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572093
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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