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nsv7045394

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,607,091

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7759 SVs from 123 studies. See in: genome view    
    Submitted genomic143,732,174-147,339,264Question Mark
    Overlapping variant regions from other studies: 4772 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):547,587-4,154,677Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045394Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1143,732,174147,339,264
    nsv7045394RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871055.3Chr1|NW_00
    3871055.3
    547,5874,154,677

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750834inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750834Submitted genomicNC_000001.11:g.143
    732174_147339264in
    v
    GRCh38 (hg38)NC_000001.11Chr1143,732,174147,339,264
    nssv18750834RemappedPerfectNW_003871055.3:g.5
    47587_4154677inv
    GRCh37.p13First PassNW_003871055.3Chr1|NW_00
    3871055.3
    547,5874,154,677

    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)
    nssv187508344e-061276268
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