Submitter Handle PACBIO Submitter SNP ID DeepVariant-CCS-hapsort.1446943 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 A/G Ancestral Allele N.D. Allele Origin N/A SNP Class SNV 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.   Fasta sequence   (Legend) >gnl|dbSNP|ss3795296072|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic GTCCCCAGTC CCTCCGCCAC GTGGG R AGCGCGGTCC TGGGCGTCTG TGCCC   Submitted Frequency for ss3795296072 There is no frequency submission for ss3795296072.   dbSNP summary of Genotypes for ss3795296072 No sufficient data to compute Hardy-weinberg probability for ss3795296072.   Submitted individual genotype for ss3795296072 There is no individual genotype data for ss3795296072.

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