A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230866



Internal ID22372053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2058649..2069872hg38UCSC Ensembl
chr5:2058763..2069986hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3811224
hg1911224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320710
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230866
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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