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nsv7049504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,452

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 34 studies. See in: genome view    
    Submitted genomic100,567,128-100,571,579Question Mark
    Overlapping variant regions from other studies: 133 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):101,183,590-101,188,041Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049504Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2100,567,128100,571,579
    nsv7049504RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2101,183,590101,188,041

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767000inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767000Submitted genomicNC_000002.12:g.100
    567128_100571579in
    v
    GRCh38 (hg38)NC_000002.12Chr2100,567,128100,571,579
    nssv18767000RemappedPerfectNC_000002.11:g.101
    183590_101188041in
    v
    GRCh37.p13First PassNC_000002.11Chr2101,183,590101,188,041

    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)
    nssv187670004e-061276268
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