A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14297646



Internal ID22135521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21890767..21913768hg38UCSC Ensembl
chr20:21871405..21894406hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3823002
hg1923002
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243808
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14297646
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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