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nsv6507806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,937

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 44 studies. See in: genome view    
    Submitted genomic56,626,578-56,633,514Question Mark
    Overlapping variant regions from other studies: 173 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):56,660,490-56,667,426Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6507806Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1656,626,57856,633,514
    nsv6507806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1656,660,49056,667,426

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18030229deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18030229Submitted genomicNC_000016.10:g.566
    26578_56633514del
    GRCh38 (hg38)NC_000016.10Chr1656,626,57856,633,514
    nssv18030229RemappedPerfectNC_000016.9:g.5666
    0490_56667426del
    GRCh37.p13First PassNC_000016.9Chr1656,660,49056,667,426

    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)
    nssv18030229<0.001339114
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