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nsv6505389

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:601

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 22 studies. See in: genome view    
    Submitted genomic38,279,504-38,280,104Question Mark
    Overlapping variant regions from other studies: 112 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):38,571,705-38,572,305Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6505389Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1538,279,50438,280,104
    nsv6505389RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1538,571,70538,572,305

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18024085deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18024085Submitted genomicNC_000015.10:g.382
    79504_38280104del
    GRCh38 (hg38)NC_000015.10Chr1538,279,50438,280,104
    nssv18024085RemappedPerfectNC_000015.9:g.3857
    1705_38572305del
    GRCh37.p13First PassNC_000015.9Chr1538,571,70538,572,305

    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)
    nssv18024085<0.001638432
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