A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539672



Internal ID20912967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86571623..86574209hg38UCSC Ensembl
chr3:86620773..86623359hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg382587
hg192587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4939n223
Supporting Variantsnssv18264050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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