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Submitted SNP(ss) Details: ss3793852670           
Submitter
HandlePACBIO
Submitter SNP IDDeepVariant-CCS-hapsort.621
RefSNP(rs#)clustering in process
Submitted Batch IDDeepVariant-CCS-hapsort
Submitted DateMar 31, 2019
Publication Cited[1] Highly-accurate long-read sequencing improves variant detection and assembly of a human genome
First entry to dbSNPMar 31 2019 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodSRX5327410
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleA/T
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|ss3793852670|allelePos=26|len=51|taxid=9606|alleles='A/T'|mol=Genomic
 CATCTAAATT AAAAGCTGGA AAAAA
 W
 TTTTATGGCT TTATGCGTTT TTCAC

  Submitted Frequency for ss3793852670 back to top
There is no frequency submission for ss3793852670.


  dbSNP summary of Genotypes for ss3793852670 back to top
No sufficient data to compute Hardy-weinberg probability for ss3793852670.


  Submitted individual genotype for ss3793852670 back to top
There is no individual genotype data for ss3793852670.