Submitter | Handle | DEVINE_LAB | Submitter SNP ID | INDEL_GP35_WGS_197503 | RefSNP(rs#) | clustering in process | Submitted Batch ID | EMORY_INDEL_GP35_WGS | Submitted Date | Jan 24, 2006 | Publication Cited | [1] An initial map of insertion and deletion (INDEL) variation in the human genome | First entry to dbSNP | Jan 24 2006 12:00:00:000AM |
| Resource Links | GenBank Accession | NT_026437
| Submitted Gene Name | N.D | Submitted Gene ID | N.D. | Submitted SNP Synonyms | N.D | Submitted linkout | N.D |
| Assay | Species | Homo sapiens | Molecular Type | Genomic | Method | METHOD_WGS | Ascertainment Samplesize | 2 | Population | N.D. |
| Allele | Observed Allele | CA/- | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | DIV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>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
There is no frequency submission for ss50017602.
No sufficient data to compute Hardy-weinberg probability for ss50017602.
There is no individual genotype data for ss50017602.
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