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nsv7074939

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,018,337

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3846 SVs from 115 studies. See in: genome view    
    Submitted genomic56,931,806-57,950,142Question Mark
    Overlapping variant regions from other studies: 3846 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):57,505,940-58,524,276Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074939Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1356,931,80657,950,142
    nsv7074939RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1357,505,94058,524,276

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753075inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753075Submitted genomicNC_000013.11:g.569
    31806_57950142inv
    GRCh38 (hg38)NC_000013.11Chr1356,931,80657,950,142
    nssv18753075RemappedPerfectNC_000013.10:g.575
    05940_58524276inv
    GRCh37.p13First PassNC_000013.10Chr1357,505,94058,524,276

    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)
    nssv187530754e-061276268
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