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nsv6778453

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:534,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1699 SVs from 82 studies. See in: genome view    
    Submitted genomic10,536,801-11,071,500Question Mark
    Overlapping variant regions from other studies: 1699 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):10,537,034-11,071,733Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6778453Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr610,536,80111,071,500
    nsv6778453RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr610,537,03411,071,733

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18520274deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18520274Submitted genomicNC_000006.12:g.105
    36801_11071500del
    GRCh38 (hg38)NC_000006.12Chr610,536,80111,071,500
    nssv18520274RemappedPerfectNC_000006.11:g.105
    37034_11071733del
    GRCh37.p13First PassNC_000006.11Chr610,537,03411,071,733

    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)
    nssv185202744e-061276168
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