| Submitter | | Handle | DEVINE_LAB | | Submitter SNP ID | INDEL_GP35_WGS_197510 | | 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_009237
| | 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 | -/TGTGTA | | Ancestral Allele | TGTGTA | | 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|ss50017607|allelePos=401|len=801|taxid=9606|alleles='-/TGTGTA'|mol=Genomic AGTTCACCAG CCTAATTCTT CATTTCTCCT GTCTCTTCAT CTAGGAAGGC ATAGTTTCTT
CCTAGAAGAT AATTAATGAC AATCTAAAGG AAGTATATGA AATATGGCCA AGTGCGGTGC
CTCATGCCTG TAACTCCCAA CACTTTGGGA GGTAAGGGCA AGAGGATCAC TTGAACCCAG
GAATTTGAGA CCAGACTGGG TAACATGGCA AAACCCTACC TCTACAAAAT ATACAAAAAA
TTAGCCAGGT GTGCTGGCAC ACATCTATGG TCCCAGCCAT TCGGGAGGAT CACCTGAGCC
CGAGGAGGTT GAGGCTGCAG TGGGCCATCA TCACACCACT GCACTCCAGT CTGAATGACA
GACTGAGACC CTGTCTCAAA AAAAAGAAAA AAAAAAATGT
N
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT ATGTGTGAGA GCGAAATGAG
AAATGTTGCA AGCAATCAAA AATCTTAAGC ATTTCTTTGA TGCTTCTAAT CACTAATTCT
ATTTTTCCTC ACTGAGGACA TCCAGATAGA AAGACATTCA CATGTATAAA GTCCCTTCTA
GACAAATAAT GGCCCTCAAA TATCTCCATG CCTTAATCTC TGGAAACTGT AAATATGTTA
GATTACACAG CAAAAGGCAA TTTAGATTAA AGATGGGATT AAGGTTGCTG ATCAGCAGGC
CTTAAAAAAT AGGAAGATTA ACCTAGATTA TCTAGGTGGG CCCAATAAAA CCTTAAAATT
GTATAATTGC AGAAGAATGT CCTGTCAGGG AGATGCTACA
There is no frequency submission for ss50017607.
No sufficient data to compute Hardy-weinberg probability for ss50017607.
There is no individual genotype data for ss50017607.
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