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nsv6715907

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:86

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 83 SVs from 16 studies. See in: genome view    
    Submitted genomic102,163,088-102,163,173Question Mark
    Overlapping variant regions from other studies: 83 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):101,881,932-101,882,017Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6715907Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3102,163,088102,163,173
    nsv6715907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3101,881,932101,882,017

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18470317deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18470317Submitted genomicNC_000003.12:g.102
    163088_102163173de
    l
    GRCh38 (hg38)NC_000003.12Chr3102,163,088102,163,173
    nssv18470317RemappedPerfectNC_000003.11:g.101
    881932_101882017de
    l
    GRCh37.p13First PassNC_000003.11Chr3101,881,932101,882,017

    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)
    nssv184703174e-061256188
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