A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546879



Internal ID20920089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144076969..144882593hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38805625
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv366n223
Supporting Variantsnssv18247024
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546879
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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