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Submitted SNP(ss) Details: ss50017590           
Submitter
HandleDEVINE_LAB
Submitter SNP IDINDEL_GP35_WGS_197490
RefSNP(rs#)rs869065109
Submitted Batch IDEMORY_INDEL_GP35_WGS
Submitted DateJan 24, 2006
Publication Cited[1] An initial map of insertion and deletion (INDEL) variation in the human genome
First entry to dbSNPJan 24 2006 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodMETHOD_WGS
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleCTTTTT/-
Ancestral AlleleCTTTTT
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|ss50017590|allelePos=401|len=800|taxid=9606|alleles='CTTTTT/-'|mol=Genomic
 CCTCACTTGT CTCATCTGTC AGACAGGGAT GGTGGTACCA AAAAAAGCCA ATGTGAAGGC
 ACAAAGCCGC AGGAGGGTAA AATAACCATG ATGATGGGAT GGGACCTCAC TTAAACATTG
 TGGTCACTTC ACTAAATGCT TTATGTGCAT CATTTAATCC TTGAAACAGC CCTAAAACAT
 AGGGAAACTG AGGCACGGAG AGGTTCTATA GCCCACCTGA GGCCTCACAG GCAGTAAGTG
 GCAGGGGTGG GACTATGGGA TTCGAGCCAG TTCTAGAGCC TCTCTGTTCT CCAGGGAGGC
 AGCACAGCCA TCCCGGGAGA GGAGAGGCAC AGGGACACGT GGGAAACAGC AGGCCTCCTT
 GGGGTTTCCT GCTGTCCTCC TGCTCATCCT CTTTCTTTTT
 N
 TTTGAGGGTG GGAACAAGAG GTGGGTGAGT GAAGTTGGAA TTAATGAGTC TGCCTGAATC
 CTAGGGAGGG GGCAGGAAGG GAAAGCCCAG GTGGGGCTCT TCAGGATTAT AGGTGTCTTG
 GAAACTGGGA GGCCAGGGGA GCACCCTTAG TGGAGGGTTC CCTATAATTT CAGTTCATTT
 TTCTCTTGCA CATTCTGCTT GAGTAGATCA ATACCCCACA AATATATCCT GTGTGTATCC
 TGAGGGGAGG CAGGGTTGAA GGAAGGTGGG AGGGAGTACA GTTGCAGATA GACGGGAGGA
 GAGAGACTGA AGATAGAGGA GAGGCGGGGA GCCATGGTAG ACCCAGGGGC CAGGAGGGTG
 GAAGAAGGCT GTGATCGAAC AGGGGCCTCA AGGCACAGC

  Submitted Frequency for ss50017590 back to top
There is no frequency submission for ss50017590.


  dbSNP summary of Genotypes for ss50017590 back to top
No sufficient data to compute Hardy-weinberg probability for ss50017590.


  Submitted individual genotype for ss50017590 back to top
There is no individual genotype data for ss50017590.

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