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nsv6507827

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,226

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 29 studies. See in: genome view    
    Submitted genomic52,570,596-52,571,821Question Mark
    Overlapping variant regions from other studies: 99 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):52,604,508-52,605,733Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507827Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1652,570,59652,571,821
    nsv6507827RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1652,604,50852,605,733

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18030401deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18030401Submitted genomicNC_000016.10:g.525
    70596_52571821del
    GRCh38 (hg38)NC_000016.10Chr1652,570,59652,571,821
    nssv18030401RemappedPerfectNC_000016.9:g.5260
    4508_52605733del
    GRCh37.p13First PassNC_000016.9Chr1652,604,50852,605,733

    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)
    nssv18030401<0.001737672
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