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nsv6521137

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:614

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 245 SVs from 57 studies. See in: genome view    
    Submitted genomic36,351,950-36,352,563Question Mark
    Overlapping variant regions from other studies: 245 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):36,842,852-36,843,465Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6521137Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,351,95036,352,563
    nsv6521137RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,842,85236,843,465

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18046353deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18046353Submitted genomicNC_000019.10:g.363
    51950_36352563del
    GRCh38 (hg38)NC_000019.10Chr1936,351,95036,352,563
    nssv18046353RemappedPerfectNC_000019.9:g.3684
    2852_36843465del
    GRCh37.p13First PassNC_000019.9Chr1936,842,85236,843,465

    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)
    nssv180463530.2774538744
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