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nsv6979538

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,102

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 29 studies. See in: genome view    
    Submitted genomic10,663,855-10,679,956Question Mark
    Overlapping variant regions from other studies: 140 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):10,567,172-10,583,273Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6979538Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1710,663,85510,679,956
    nsv6979538RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1710,567,17210,583,273

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18406507deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18406507Submitted genomicNC_000017.11:g.106
    63855_10679956del
    GRCh38 (hg38)NC_000017.11Chr1710,663,85510,679,956
    nssv18406507RemappedPerfectNC_000017.10:g.105
    67172_10583273del
    GRCh37.p13First PassNC_000017.10Chr1710,567,17210,583,273

    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)
    nssv184065071.8e-055276248
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