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Submitted SNP(ss) Details: ss552065179           
Submitter
HandleLUNTER
Submitter SNP IDCEU_10_107937255-107937256
RefSNP(rs#)rs68166392
Submitted Batch IDindel_calls_from_1000_genomes_pilot_1_CEU
Submitted DateNov 21, 2012
Publication Cited[1] The Origin, evolution and functional impact of short insertion-deletion variants identified in 179 human genomes
First entry to dbSNPNov 21 2012 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA_SHORT_SEQUENCE_DATA
Ascertainment Samplesize358
PopulationN.D.
Allele
Observed Allele-/TT
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss552065179|allelePos=26|len=51|taxid=9606|alleles='-/TT'|mol=Genomic
 AGGGGCAATT TTTTTTTCTT TTTTC
 N
 TTTTCTTTTT TTTTTTTTGA GATGG

  Submitted Frequency for ss552065179 back to top
There is no frequency submission for ss552065179.


  dbSNP summary of Genotypes for ss552065179 back to top
No sufficient data to compute Hardy-weinberg probability for ss552065179.


  Submitted individual genotype for ss552065179 back to top
There is no individual genotype data for ss552065179.

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