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nsv6988144

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:169,376

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1484 SVs from 79 studies. See in: genome view    
    Submitted genomic89,658,140-89,827,515Question Mark
    Overlapping variant regions from other studies: 1484 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):89,724,548-89,893,923Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6988144Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1689,658,14089,827,515
    nsv6988144RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1689,724,54889,893,923

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624973duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624973Submitted genomicNC_000016.10:g.896
    58140_89827515dup
    GRCh38 (hg38)NC_000016.10Chr1689,658,14089,827,515
    nssv18624973RemappedPerfectNC_000016.9:g.8972
    4548_89893923dup
    GRCh37.p13First PassNC_000016.9Chr1689,724,54889,893,923

    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)
    nssv186249737e-062271978
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