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nsv7003315

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,573

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 35 studies. See in: genome view    
    Submitted genomic53,697,826-53,700,398Question Mark
    Overlapping variant regions from other studies: 143 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):54,201,080-54,203,652Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7003315Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,697,82653,700,398
    nsv7003315RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,201,08054,203,652

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18425921deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18425921Submitted genomicNC_000019.10:g.536
    97826_53700398del
    GRCh38 (hg38)NC_000019.10Chr1953,697,82653,700,398
    nssv18425921RemappedPerfectNC_000019.9:g.5420
    1080_54203652del
    GRCh37.p13First PassNC_000019.9Chr1954,201,08054,203,652

    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)
    nssv184259214e-061275200
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