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Submitted SNP(ss) Details: ss3063573498           
Submitter
HandleMCHAISSO
Submitter SNP IDHG0051494
RefSNP(rs#)rs143445210
Submitted Batch IDHG00514
Submitted DateSep 15, 2017
Publication Cited[1] Multi-platform discovery of haplotype-resolved structural variation in human genomes
First entry to dbSNPSep 15 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodUNIFIEDCALLSET
Ascertainment Samplesize46
PopulationCHS-PUR-YRI
Allele
Observed AlleleAC/-
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|ss3063573498|allelePos=26|len=51|taxid=9606|alleles='AC/-'|mol=Genomic
 CACACACCTG GACAAACACA CCTGG
 N
 ACACACACCT AGACACACAC ACCTA

  Submitted Frequency for ss3063573498 back to top
There is no frequency submission for ss3063573498.


  dbSNP summary of Genotypes for ss3063573498 back to top
No sufficient data to compute Hardy-weinberg probability for ss3063573498.


  Submitted individual genotype for ss3063573498 back to top
There is no individual genotype data for ss3063573498.