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nsv6875386

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,275

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 268 SVs from 42 studies. See in: genome view    
    Submitted genomic15,228,550-15,241,824Question Mark
    Overlapping variant regions from other studies: 274 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):15,228,548-15,241,822Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875386Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr915,228,55015,241,824
    nsv6875386RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr915,228,54815,241,822

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18567126deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18567126Submitted genomicNC_000009.12:g.152
    28550_15241824del
    GRCh38 (hg38)NC_000009.12Chr915,228,55015,241,824
    nssv18567126RemappedPerfectNC_000009.11:g.152
    28548_15241822del
    GRCh37.p13First PassNC_000009.11Chr915,228,54815,241,822

    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)
    nssv185671261.8e-055276108
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