| Submitter | | Handle | PACBIO | | Submitter SNP ID | DeepVariant-CCS-hapsort.1827198 | | RefSNP(rs#) | clustering in process | | Submitted Batch ID | DeepVariant-CCS-hapsort | | Submitted Date | Mar 31, 2019 | | Publication Cited | [1] Highly-accurate long-read sequencing improves variant detection and assembly of a human genome | | First entry to dbSNP | Mar 31 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 | 2 | | Population | N.D. |
| | Allele | | Observed Allele | -/T | | 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|ss3795675686|allelePos=26|len=51|taxid=9606|alleles='-/T'|mol=Genomic CAGGTGGAAG CCACCGCACC CTGCC
N
TTTTTTTTTT TTTTTTTTTT TTGAC
There is no frequency submission for ss3795675686.
No sufficient data to compute Hardy-weinberg probability for ss3795675686.
There is no individual genotype data for ss3795675686.
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