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Submitted SNP(ss) Details: ss551224567           
Submitter
HandleLUNTER
Submitter SNP IDCEU_3_37822802-37822803
RefSNP(rs#)rs59945410
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 AlleleGT/-
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|ss551224567|allelePos=26|len=51|taxid=9606|alleles='GT/-'|mol=Genomic
 TGGGTGTGTG TGTGTGTGCG TGCGC
 N
 GTGTGTGTGT GTATGTGACT TCCTT

  Submitted Frequency for ss551224567 back to top
There is no frequency submission for ss551224567.


  dbSNP summary of Genotypes for ss551224567 back to top
No sufficient data to compute Hardy-weinberg probability for ss551224567.


  Submitted individual genotype for ss551224567 back to top
There is no individual genotype data for ss551224567.

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