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nsv6809392

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,228

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 26 studies. See in: genome view    
    Submitted genomic2,762,767-2,765,994Question Mark
    Overlapping variant regions from other studies: 143 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):2,802,401-2,805,628Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6809392Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr72,762,7672,765,994
    nsv6809392RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr72,802,4012,805,628

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18540166deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18540166Submitted genomicNC_000007.14:g.276
    2767_2765994del
    GRCh38 (hg38)NC_000007.14Chr72,762,7672,765,994
    nssv18540166RemappedPerfectNC_000007.13:g.280
    2401_2805628del
    GRCh37.p13First PassNC_000007.13Chr72,802,4012,805,628

    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)
    nssv185401662.5e-057274900
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