A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3553499



Internal ID22422380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168692356..168695795hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8248n152
Supporting Variantsnssv14459996
SamplesHG00513
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3553499
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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