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nsv6482144

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,432

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 35 studies. See in: genome view    
    Submitted genomic20,746,151-20,768,582Question Mark
    Overlapping variant regions from other studies: 124 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):21,214,310-21,236,741Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6482144Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1420,746,15120,768,582
    nsv6482144RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1421,214,31021,236,741

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18016569deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18016569Submitted genomicNC_000014.9:g.2074
    6151_20768582del
    GRCh38 (hg38)NC_000014.9Chr1420,746,15120,768,582
    nssv18016569RemappedPerfectNC_000014.8:g.2121
    4310_21236741del
    GRCh37.p13First PassNC_000014.8Chr1421,214,31021,236,741

    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)
    nssv18016569<0.001139236
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