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nsv6516839

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
    Submitted genomic43,652,001-43,653,800Question Mark
    Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):44,156,153-44,157,952Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6516839Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1943,652,00143,653,800
    nsv6516839RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1944,156,15344,157,952

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18048116deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18048116Submitted genomicNC_000019.10:g.436
    52001_43653800del
    GRCh38 (hg38)NC_000019.10Chr1943,652,00143,653,800
    nssv18048116RemappedPerfectNC_000019.9:g.4415
    6153_44157952del
    GRCh37.p13First PassNC_000019.9Chr1944,156,15344,157,952

    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)
    nssv18048116<0.001138500
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