A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14300768



Internal ID22310165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40637157..40643494hg38UCSC Ensembl
chr20:39265797..39272134hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg386338
hg196338
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3240494
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14300768
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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