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nsv6505159

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,511

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 21 studies. See in: genome view    
    Submitted genomic92,476,683-92,479,193Question Mark
    Overlapping variant regions from other studies: 135 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):93,019,913-93,022,423Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6505159Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1592,476,68392,479,193
    nsv6505159RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1593,019,91393,022,423

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18027297deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18027297Submitted genomicNC_000015.10:g.924
    76683_92479193del
    GRCh38 (hg38)NC_000015.10Chr1592,476,68392,479,193
    nssv18027297RemappedPerfectNC_000015.9:g.9301
    9913_93022423del
    GRCh37.p13First PassNC_000015.9Chr1593,019,91393,022,423

    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)
    nssv18027297<0.001239252
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