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nsv7050772

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,808

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Submitted genomic172,197,867-172,203,674Question Mark
    Overlapping variant regions from other studies: 103 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):171,915,657-171,921,464Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050772Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3172,197,867172,203,674
    nsv7050772RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3171,915,657171,921,464

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18769916inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18769916Submitted genomicNC_000003.12:g.172
    197867_172203674in
    v
    GRCh38 (hg38)NC_000003.12Chr3172,197,867172,203,674
    nssv18769916RemappedPerfectNC_000003.11:g.171
    915657_171921464in
    v
    GRCh37.p13First PassNC_000003.11Chr3171,915,657171,921,464

    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)
    nssv187699167e-062274752
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