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nsv6987573

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,905

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 187 SVs from 32 studies. See in: genome view    
    Submitted genomic75,538,037-75,542,941Question Mark
    Overlapping variant regions from other studies: 187 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):73,534,118-73,539,022Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6987573Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,538,03775,542,941
    nsv6987573RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,534,11873,539,022

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18415254deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18415254Submitted genomicNC_000017.11:g.755
    38037_75542941del
    GRCh38 (hg38)NC_000017.11Chr1775,538,03775,542,941
    nssv18415254RemappedPerfectNC_000017.10:g.735
    34118_73539022del
    GRCh37.p13First PassNC_000017.10Chr1773,534,11873,539,022

    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)
    nssv184152544e-061276096
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