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nsv6995360

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,723

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 29 studies. See in: genome view    
    Submitted genomic72,961,103-72,975,825Question Mark
    Overlapping variant regions from other studies: 141 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):70,957,242-70,971,964Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995360Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1772,961,10372,975,825
    nsv6995360RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1770,957,24270,971,964

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18414086deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18414086Submitted genomicNC_000017.11:g.729
    61103_72975825del
    GRCh38 (hg38)NC_000017.11Chr1772,961,10372,975,825
    nssv18414086RemappedPerfectNC_000017.10:g.709
    57242_70971964del
    GRCh37.p13First PassNC_000017.10Chr1770,957,24270,971,964

    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)
    nssv184140864e-061276258
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