| Submitter | | Handle | DEVINE_LAB | | Submitter SNP ID | INDEL_GP35_WGS_197484 | | 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 | -/CTA | | Ancestral Allele | CTA | | 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|ss50017585|allelePos=401|len=801|taxid=9606|alleles='-/CTA'|mol=Genomic AGCCTCCTTG TCACTGATCA GCCTATGTGG GTTGCCTCTG AGCATATTGT TCCTTTAAAA
ACCAAAGTGT AAATGTCTCA CCCAAAAGGC CAAGCTGTTG CTCTGTCCAG TCTAGACTGT
GCCTGTGAGG CTAGCAATGC CACCCTCCCT CTGTAACAGT GCCCTGGGGT ATGGGTGGCA
ACAGGACAAC CAGGTGCTTG TGCTGGGAAG CGGGTTTTTT TAAGAGAGCA CTGCCTTTTA
TTTACAGACA GCTTTATCAG TACATGGCCA TGTTCCTGCC GACCTTGAGG ACTCTTTACC
AAACAATCCT GCTGCTGAAT ATTCACTTCC TTCCACATGA ATTTGCTCTT AGGGATTGGA
GGAGGGGTGG AAATGCTTTC AACCAGTCTC CATAATCTAG
N
GCTTCTTGTG CACCTGGGGT ACCCACAAAC AAACCCTGTT CTCACTCTGG TTTTCCTTTT
CCTGATTAAC ATCCCCACAA ACCTACTGGA TTTAAGACAA ACCCAGAAGT CATCATTTCT
GCTGCTTCTC TCTATCCGTC TATCTCTAAG TGATTATCAA GCCTTATTAC TGATTTTGCT
TTCACCGAAG CCCTGCTTCC TTTCCCCTGA CTAACTCCTT ATTTTCCATT CCATTCATCA
CTGTCCTGGT TCAGGTCTTA ACATCTCTTC CCTGGACGGT TTCAGCCTCC CCCAACTGAT
CTTTTCTTGT CCAGCCAGGA ATCTGTTACT CCCTTAATGA GGGAGCATCA ATGAGTTCCT
TTTGCCTAAT ATGTAAAAAT CAAAATTCCT TCGTGTGACA
There is no frequency submission for ss50017585.
No sufficient data to compute Hardy-weinberg probability for ss50017585.
There is no individual genotype data for ss50017585.
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