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nsv7004207

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,075,080

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11870 SVs from 112 studies. See in: genome view    
    Submitted genomic77,635,799-79,710,878Question Mark
    Overlapping variant regions from other studies: 11848 SVs from 112 studies. See in: genome view    
    Remapped(Score: Good):75,347,755-77,470,878Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7004207Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1877,635,79979,710,878
    nsv7004207RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1875,347,75577,470,878

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18420664deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18420664Submitted genomicNC_000018.10:g.776
    35799_79710878del
    GRCh38 (hg38)NC_000018.10Chr1877,635,79979,710,878
    nssv18420664RemappedGoodNC_000018.9:g.7534
    7755_77470878del
    GRCh37.p13First PassNC_000018.9Chr1875,347,75577,470,878

    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)
    nssv184206644e-061276150
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