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Submitted SNP(ss) Details: ss50017602           
Submitter
HandleDEVINE_LAB
Submitter SNP IDINDEL_GP35_WGS_197503
RefSNP(rs#)clustering in process
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 AlleleCA/-
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|ss50017602|allelePos=401|len=800|taxid=9606|alleles='CA/-'|mol=Genomic
 CAATCACAGA AACACACACA CACAGACACA TAGCCACAGA CACATCCTCA GTCTAGATAG
 AAACACCTAG ACACACAGAC ACATATAGAC TCAGACAAAC AGAGAAACAT CACACACACA
 GCCTCACCCA CAACCACATG CAAACACACA GAAACACCTA GGTACCCTAA CACACATAGA
 CTCAGACACA CAGACTCTCA GACTCACATT GACTCAGGGA CACACAAACA CAGAAGCACA
 CACATACACA GACACACACA GACATATCCA CAGCCATATG CAGACACAAA GACAGAACTA
 CTTAGACACA CAGACATATC CACAGCCATA TGCAGACACA AAGACAGAAC TACCTAGACA
 CACAGACACA CATGCACAGA CACACACACA GACACACACG
 N
 CACACACACA CAGACACACA TGGTCACACA CAAACACACA GAGACACATG CACGCGGACA
 CACACAGACA TACCCACACA GAGACACACA CACACAGACA TACCCACGCA GCCACACACA
 CACACGCAGA CACACAGATG TACACACAGA GACACACACA TATACAGACA CACACAAACA
 CACACAGAGA CACACACACA CATAGTCACA AACAGACATA CCCACACAGA GACACACACA
 CGCAGAGACA CACCCACGCA GCCACACACA CACACAGACA CACACAAACA CACGTGGTGG
 AGTCCCTCTC ACTCTGGGCC ACACAGACGC CACCAAAGGC TGCACATCTG ACTTCCCCAA
 CCTCCGGGTT GGGGCCTGGC AGGGAGGCAA GGTGTGGCA

  Submitted Frequency for ss50017602 back to top
There is no frequency submission for ss50017602.


  dbSNP summary of Genotypes for ss50017602 back to top
No sufficient data to compute Hardy-weinberg probability for ss50017602.


  Submitted individual genotype for ss50017602 back to top
There is no individual genotype data for ss50017602.

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