A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14297556



Internal ID22276343
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3234813
Supporting Variants
SamplesNA19239
Known GenesDTD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14297556
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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