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nsv6931314

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:710,957

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2146 SVs from 88 studies. See in: genome view    
    Submitted genomic23,578,620-24,289,576Question Mark
    Overlapping variant regions from other studies: 2146 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):24,152,759-24,863,714Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6931314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1323,578,62024,289,576
    nsv6931314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1324,152,75924,863,714

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18600050duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18600050Submitted genomicNC_000013.11:g.235
    78620_24289576dup
    GRCh38 (hg38)NC_000013.11Chr1323,578,62024,289,576
    nssv18600050RemappedPerfectNC_000013.10:g.241
    52759_24863714dup
    GRCh37.p13First PassNC_000013.10Chr1324,152,75924,863,714

    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)
    nssv186000504e-061275450
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