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Submitted SNP(ss) Details: ss3796796008           
Submitter
HandlePACBIO
Submitter SNP IDDeepVariant-CCS-hapsort.2949986
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 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|ss3796796008|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 TGCTCCCCCG AGTTGGGACT AGGGC
 Y
 TCAATTTCAC TTCTTAAAAA AAATC

  Submitted Frequency for ss3796796008 back to top
There is no frequency submission for ss3796796008.


  dbSNP summary of Genotypes for ss3796796008 back to top
No sufficient data to compute Hardy-weinberg probability for ss3796796008.


  Submitted individual genotype for ss3796796008 back to top
There is no individual genotype data for ss3796796008.