A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3553591



Internal ID22422470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168390177..168393080hg38UCSC Ensembl
chr6:168790857..168793760hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382904
hg192904
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14461137
SamplesNA19238
Known Genes
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3553591
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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