Submitter | Handle | PACBIO | Submitter SNP ID | DeepVariant-CCS.1630398 | RefSNP(rs#) | clustering in process | Submitted Batch ID | DeepVariant-CCS | Submitted Date | Mar 30, 2019 | Publication Cited | [1] Highly-accurate long-read sequencing improves variant detection and assembly of a human genome | First entry to dbSNP | Mar 30 2019 12:00:00:000AM |
| Resource Links | 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 | SRX5327410 | Ascertainment Samplesize | N.D. | Population | N.D. |
| Allele | Observed Allele | AAAA/- | Ancestral Allele | N.D. | Allele Origin | N/A | SNP Class | DIV | CpG Code | N.D. |
| Validation | Validation Status | Not Validated | HWE Goodness of Fit | not applicable | Homozygote Detected | | PCR Confirmed | | In Expressed Sequence | |
| Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss3790606603|allelePos=26|len=51|taxid=9606|alleles='AAAA/-'|mol=Genomic GGGCGACAGA GCGAGACTCC GTCTC
N
AAAAAAAAAA AAAAAAAAAA AAAAA
There is no frequency submission for ss3790606603.
No sufficient data to compute Hardy-weinberg probability for ss3790606603.
There is no individual genotype data for ss3790606603.
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