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Submitted SNP(ss) Details: ss550903134           
Submitter
HandleLUNTER
Submitter SNP IDCEU_1_802796-802797
RefSNP(rs#)rs141564386
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-/CAT
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|ss550903134|allelePos=26|len=51|taxid=9606|alleles='-/CAT'|mol=Genomic
 AGATTAACAT CCAACCTGTA CAGGA
 N
 CATCAAATCT CCCCATCCCT CATTC

  Submitted Frequency for ss550903134 back to top
There is no frequency submission for ss550903134.


  dbSNP summary of Genotypes for ss550903134 back to top
No sufficient data to compute Hardy-weinberg probability for ss550903134.


  Submitted individual genotype for ss550903134 back to top
There is no individual genotype data for ss550903134.