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nsv7010883

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,691

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 215 SVs from 35 studies. See in: genome view    
    Submitted genomic46,953,960-46,959,650Question Mark
    Overlapping variant regions from other studies: 215 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):44,533,923-44,539,613Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010883Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1846,953,96046,959,650
    nsv7010883RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1844,533,92344,539,613

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18418184deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18418184Submitted genomicNC_000018.10:g.469
    53960_46959650del
    GRCh38 (hg38)NC_000018.10Chr1846,953,96046,959,650
    nssv18418184RemappedPerfectNC_000018.9:g.4453
    3923_44539613del
    GRCh37.p13First PassNC_000018.9Chr1844,533,92344,539,613

    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)
    nssv184181844e-061276048
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