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nsv6960945

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:189

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Submitted genomic84,641,053-84,641,241Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):85,184,284-85,184,472Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6960945Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1584,641,05384,641,241
    nsv6960945RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1585,184,28485,184,472

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18397128deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18397128Submitted genomicNC_000015.10:g.846
    41053_84641241del
    GRCh38 (hg38)NC_000015.10Chr1584,641,05384,641,241
    nssv18397128RemappedPerfectNC_000015.9:g.8518
    4284_85184472del
    GRCh37.p13First PassNC_000015.9Chr1585,184,28485,184,472

    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)
    nssv183971280.0051327260448
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