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nsv6534729

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,215

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 32 studies. See in: genome view    
    Submitted genomic48,323,295-48,324,509Question Mark
    Overlapping variant regions from other studies: 89 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):48,826,552-48,827,766Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6534729Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,323,29548,324,509
    nsv6534729RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1948,826,55248,827,766

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18048377deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18048377Submitted genomicNC_000019.10:g.483
    23295_48324509del
    GRCh38 (hg38)NC_000019.10Chr1948,323,29548,324,509
    nssv18048377RemappedPerfectNC_000019.9:g.4882
    6552_48827766del
    GRCh37.p13First PassNC_000019.9Chr1948,826,55248,827,766

    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)
    nssv18048377<0.0011637694
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