A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567709



Internal ID20940780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170408581..170409029hg38UCSC Ensembl
chr3:170126369..170126817hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5083n223
Supporting Variantsnssv18260514
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567709
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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