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nsv6927631

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,482

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 31 studies. See in: genome view    
    Submitted genomic21,638,470-21,641,951Question Mark
    Overlapping variant regions from other studies: 153 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):21,791,404-21,794,885Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6927631Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,638,47021,641,951
    nsv6927631RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,791,40421,794,885

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18359511deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18359511Submitted genomicNC_000012.12:g.216
    38470_21641951del
    GRCh38 (hg38)NC_000012.12Chr1221,638,47021,641,951
    nssv18359511RemappedPerfectNC_000012.11:g.217
    91404_21794885del
    GRCh37.p13First PassNC_000012.11Chr1221,791,40421,794,885

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv183595114e-061274774
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