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Submitted SNP(ss) Details: ss3788980067           
Submitter
HandlePACBIO
Submitter SNP IDDeepVariant-CCS.606
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 AlleleT/C
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
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|ss3788980067|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 GGACTGAGGC CAGTGCTTTC AACCA
 Y
 ACTCACTTTT CACTGTGTTC AGAGG

  Submitted Frequency for ss3788980067 back to top
There is no frequency submission for ss3788980067.


  dbSNP summary of Genotypes for ss3788980067 back to top
No sufficient data to compute Hardy-weinberg probability for ss3788980067.


  Submitted individual genotype for ss3788980067 back to top
There is no individual genotype data for ss3788980067.