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Submitted SNP(ss) Details: ss550903122           
Submitter
HandleLUNTER
Submitter SNP IDCEU_1_759002-759003
RefSNP(rs#)rs59306077
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 AlleleAT/-
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|ss550903122|allelePos=26|len=51|taxid=9606|alleles='AT/-'|mol=Genomic
 GCAAAGCATA TGGCTCTGGT GAGAC
 N
 GTGTGAGGAG CTGAGAATGA GACGG

  Submitted Frequency for ss550903122 back to top
There is no frequency submission for ss550903122.


  dbSNP summary of Genotypes for ss550903122 back to top
No sufficient data to compute Hardy-weinberg probability for ss550903122.


  Submitted individual genotype for ss550903122 back to top
There is no individual genotype data for ss550903122.