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nsv6535248

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:242

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 16 studies. See in: genome view    
    Submitted genomic79,837,486-79,837,727Question Mark
    Overlapping variant regions from other studies: 134 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):77,811,285-77,811,526Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6535248Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1779,837,48679,837,727
    nsv6535248RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1777,811,28577,811,526

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18038637deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18038637Submitted genomicNC_000017.11:g.798
    37486_79837727del
    GRCh38 (hg38)NC_000017.11Chr1779,837,48679,837,727
    nssv18038637RemappedPerfectNC_000017.10:g.778
    11285_77811526del
    GRCh37.p13First PassNC_000017.10Chr1777,811,28577,811,526

    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)
    nssv180386370.0026936318
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