NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss327276797           
Submitter
Handle1000GENOMES
Submitter SNP IDJPTCHB_chr10_107937255_indel
RefSNP(rs#)rs68166392
Submitted Batch IDJPTCHB_low_coverage_pilot_indel
Submitted DateMar 11, 2011
Publication Cited20980555 20980557 20981092
First entry to dbSNPMar 11 2011 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodLOW_COVERAGE_PILOT_INDELS
Ascertainment Samplesize120
Populationpilot_1_CHB+JPT_low_coverage_panel
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|ss327276797|allelePos=51|len=101|taxid=9606|alleles='-/TT'|mol=Genomic
 AATTCTGTAG AATACACTTA GTAAGAGGGG CAATTTTTTT TTCTTTTTTC
 N
 TTTTCTTTTT TTTTTTTTGA GATGGAATCT CGCTCTGTTG CCCAGGCTGG

  Submitted Frequency for ss327276797 back to top
There is no frequency submission for ss327276797.


  dbSNP summary of Genotypes for ss327276797 back to top
No sufficient data to compute Hardy-weinberg probability for ss327276797.


  Submitted individual genotype for ss327276797 back to top
There is no individual genotype data for ss327276797.

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement