| Submitter | | Handle | DEVINE_LAB | | Submitter SNP ID | INDEL_GP35_WGS_197480 | | 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_005612
| | 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 | -/TG | | 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|ss50017582|allelePos=401|len=801|taxid=9606|alleles='-/TG'|mol=Genomic TCTTCTTGAC TTTGCCAAGA ACAAAGAATT TCCATGTCAG AGTGTGCCTA TTTTGTGAAG
TCCGTTATAA AAGTTGTTCT TGAAAACACT GCCAACCACG TGAAAACATG ATCTGACTTT
GGGTGAGATA ATAATGTAGG TGGGTAAAAT TTAGACTAAC CAGCCCACTC TCTCTCCAGG
TGCCATCAAC AAATATCCCA CCGAAGATAT GAAAGCCACA TGTGTTAACA TGACCTCTCC
CAACCCAGAG AACGGTGGCA CAGAAAACAC TGTATTGTGA GTTGAGAAAT TCCAAGTTTG
GGTAATACCA CAACTGGAAA CAGTTCTTAA GAAAACTGTG AAATGAATAG CATTTTAGTT
TTCAAGATCC AAGTGTGTGT TTTTGTGTGT GTGTGTGTGT
N
GTGTGTGTGT TTTAAATGCT ACTCGTTTGT GATGATAGCA TAGGTCTGAA ATTAATCGCA
GATAGAACAG GACTTATATT TGAAAGAACT TTGCTTCCAT TTCTGTTTCT TTTACCAAAA
GTAGCCTCCT ATTAGTAACT TCTCAGTAAG TAGATAACAT AACTCCAATA TTGGGTACTG
CCAAAACAGA AAACTTATAT CAAAGATTCC ATGTAACAAT TTTAGAGCAG AATAAAAACA
TAAAAAACAA AACAAAATAT TTGGCCATTT AGAAAGCAAA ACACATATGA AGATTGGCAG
GAAGGATTCT TTCAAGTTTG ATTTTACAAA GTACAACCCT AAGTACTCAA TAAAAATTTA
ATGATAGAAA TTATACTGGT TTGGAATTCT AAACTGCGGA
There is no frequency submission for ss50017582.
No sufficient data to compute Hardy-weinberg probability for ss50017582.
There is no individual genotype data for ss50017582.
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