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nsv6997487

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22,057

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 37 studies. See in: genome view    
    Submitted genomic65,322,755-65,344,811Question Mark
    Overlapping variant regions from other studies: 154 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):65,356,658-65,378,714Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6997487Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1665,322,75565,344,811
    nsv6997487RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1665,356,65865,378,714

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18401790deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18401790Submitted genomicNC_000016.10:g.653
    22755_65344811del
    GRCh38 (hg38)NC_000016.10Chr1665,322,75565,344,811
    nssv18401790RemappedPerfectNC_000016.9:g.6535
    6658_65378714del
    GRCh37.p13First PassNC_000016.9Chr1665,356,65865,378,714

    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)
    nssv184017904e-061276244
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