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Submitted SNP(ss) Details: ss3790496039           
Submitter
HandlePACBIO
Submitter SNP IDDeepVariant-CCS.1519657
RefSNP(rs#)clustering in process
Submitted Batch IDDeepVariant-CCS
Submitted DateMar 30, 2019
Publication Cited[1] Highly-accurate long-read sequencing improves variant detection and assembly of a human genome
First entry to dbSNPMar 30 2019 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodSRX5327410
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed Allele-/TG
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Homozygote Detected
PCR Confirmed
In Expressed Sequence
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3790496039|allelePos=26|len=51|taxid=9606|alleles='-/TG'|mol=Genomic
 ATACAATTAT TTCACTGGTT TTATA
 N
 TGTGTGTGTG TGTGTGTGTA TGGAA

  Submitted Frequency for ss3790496039 back to top
There is no frequency submission for ss3790496039.


  dbSNP summary of Genotypes for ss3790496039 back to top
No sufficient data to compute Hardy-weinberg probability for ss3790496039.


  Submitted individual genotype for ss3790496039 back to top
There is no individual genotype data for ss3790496039.

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