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nsv6404392

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:511

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Submitted genomic49,743,567-49,744,077Question Mark
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):49,711,280-49,711,790Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6404392Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,743,56749,744,077
    nsv6404392RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,711,28049,711,790

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18142823deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18142823Submitted genomicNC_000006.12:g.497
    43567_49744077del
    GRCh38 (hg38)NC_000006.12Chr649,743,56749,744,077
    nssv18142823RemappedPerfectNC_000006.11:g.497
    11280_49711790del
    GRCh37.p13First PassNC_000006.11Chr649,711,28049,711,790

    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)
    nssv18142823<0.0013037496
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