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Submitted SNP(ss) Details: ss3065395826           
Submitter
HandleMCHAISSO
Submitter SNP IDNA19240113452
RefSNP(rs#)rs762344516
Submitted Batch IDNA19240
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 Allele-/T
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|ss3065395826|allelePos=26|len=51|taxid=9606|alleles='-/T'|mol=Genomic
 TGTCATTTCA TTTCTTTTTC TTTTC
 N
 TTTTTTTTTT TTTTTAGGAC AAAAT

  Submitted Frequency for ss3065395826 back to top
There is no frequency submission for ss3065395826.


  dbSNP summary of Genotypes for ss3065395826 back to top
No sufficient data to compute Hardy-weinberg probability for ss3065395826.


  Submitted individual genotype for ss3065395826 back to top
There is no individual genotype data for ss3065395826.