A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3234813



Internal ID22373128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18610914..18615178hg38UCSC Ensembl
chr20:18591558..18595822hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg384265
hg194265
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14297556
SamplesNA19239
Known GenesDTD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3234813
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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