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Submitted SNP(ss) Details: ss3064725070           
Submitter
HandleMCHAISSO
Submitter SNP IDHG00733339128
RefSNP(rs#)rs377299834
Submitted Batch IDHG00733
Submitted DateSep 15, 2017
Publication Cited[1] Multi-platform discovery of haplotype-resolved structural variation in human genomes
First entry to dbSNPSep 15 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodUNIFIEDCALLSET
Ascertainment Samplesize46
PopulationCHS-PUR-YRI
Allele
Observed AlleleT/-
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Homozygote Detected
PCR Confirmed
In Expressed Sequence
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3064725070|allelePos=26|len=51|taxid=9606|alleles='T/-'|mol=Genomic
 CAGAGGACAG TATGCTCAGA ATGGA
 N
 TTTTTTTTTT TAAGAGGCTG GATCT

  Submitted Frequency for ss3064725070 back to top
There is no frequency submission for ss3064725070.


  dbSNP summary of Genotypes for ss3064725070 back to top
No sufficient data to compute Hardy-weinberg probability for ss3064725070.


  Submitted individual genotype for ss3064725070 back to top
There is no individual genotype data for ss3064725070.

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