U.S. flag

An official website of the United States government

nsv6652402

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 21 studies. See in: genome view    
    Submitted genomic63,782,401-63,785,600Question Mark
    Overlapping variant regions from other studies: 123 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):64,248,072-64,251,271Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6652402Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr163,782,40163,785,600
    nsv6652402RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr164,248,07264,251,271

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18409830deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18409830Submitted genomicNC_000001.11:g.637
    82401_63785600del
    GRCh38 (hg38)NC_000001.11Chr163,782,40163,785,600
    nssv18409830RemappedPerfectNC_000001.10:g.642
    48072_64251271del
    GRCh37.p13First PassNC_000001.10Chr164,248,07264,251,271

    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)
    nssv184098304e-061276160
    Support Center