U.S. flag

An official website of the United States government

nsv7005672

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 351 SVs from 28 studies. See in: genome view    
    Submitted genomic75,696,626-75,696,708Question Mark
    Overlapping variant regions from other studies: 351 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):73,408,581-73,408,663Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7005672Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1875,696,62675,696,708
    nsv7005672RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1873,408,58173,408,663

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18420065deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18420065Submitted genomicNC_000018.10:g.756
    96626_75696708del
    GRCh38 (hg38)NC_000018.10Chr1875,696,62675,696,708
    nssv18420065RemappedPerfectNC_000018.9:g.7340
    8581_73408663del
    GRCh37.p13First PassNC_000018.9Chr1873,408,58173,408,663

    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)
    nssv184200650.0358688247554
    Support Center