| Submitter | | Handle | DEVINE_LAB | | Submitter SNP ID | INDEL_GP35_WGS_659597 | | 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_010498
| | 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 | (LARGEDELETION)/- | | Ancestral Allele | - | | Allele Origin | N/A | | SNP Class | Named | | CpG Code | N.D. |
| | | Variation | | Frequency Submission | N.D. | | Genotype Summary | N.D. | | Genotype Submission | N.D. | | Haplotype | N.D. |
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| Comment | | largedeletion=ctgaggttgggagttcgagaccagcctgaccaacgtggagaaaccccatc |
>gnl|dbSNP|ss50366203|allelePos=401|len=800|taxid=9606|alleles='(LARGEDELETION)/-'|mol=Genomic TGCCATTAGA GGCAGCCTGG AATGGCCAGA TCTGTTTCCT TGTGCTCTGT TTTAATTTAG
TTTTCATCTG TATAGAAGTT GTACATAGCC TAAAATTTAA AACCTCAAAT ACCAGTATTT
CTACAATTAA TTTCAATGGA AAGAGGAAAC TTCTGCCCCA CTCCTTCCCA TTCTCCATGA
GCCTAAACTT TCTGTGCTTT CGTCTGTGCT TTGCTGATCG CCTCCACCTT TCTAGACCAC
ATGGTCATAC CACAGTTTCT TTCTTTTCTT ATTTAAAAAA CACCGTGGCC AGGCGCAGTG
GCTCACGCCT ATAATCCCAG CACTTTGGGA GGCCAAGGCA GGCGGATCAC CTGAGGTTGG
GAGTTCGAGA CCAGCCTGAC CAACGTGGAG AAACCCCATC
N
TCTACTAAAA ATACAAAATT AGCCGGGTGT GGTGGCACAT GTCTGTAATC CCAGCTACTT
GGGAGGCTGA GGCAGGAGAA TCACCTGAAC CCGGGAGGTG GGGGTTGTGG TGAGCCAAGA
TCGCACCATT GCACTATAGC CTGGGCAACA AGAGCGAAAC TCCATCTCAA AAAAAAAAAA
AAAAGTTAAC ACATTAGTTA TTCTCTTCCT ACTGTAAAGG ATGAGAATTT AGCTCTCTCA
TGGCACCACT CCCAGCCCCA TGGCTCGTGT TTCTCCTCCC ACCCTCCCAG TAGCACCATT
TCAATAGGTG GTGTTTATAA TGTAAGGACG CATAAGTGTC ATTTACCACT GACTATTTCT
TTTTAATAAC TTGGTTTCCC TGGAGTTAAT AATAGTTCC
There is no frequency submission for ss50366203.
No sufficient data to compute Hardy-weinberg probability for ss50366203.
There is no individual genotype data for ss50366203.
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