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nsv7063743

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,529

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 530 SVs from 56 studies. See in: genome view    
    Submitted genomic19,172,900-19,248,428Question Mark
    Overlapping variant regions from other studies: 536 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):19,172,898-19,248,426Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063743Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr919,172,90019,248,428
    nsv7063743RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr919,172,89819,248,426

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18785793inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18785793Submitted genomicNC_000009.12:g.191
    72900_19248428inv
    GRCh38 (hg38)NC_000009.12Chr919,172,90019,248,428
    nssv18785793RemappedPerfectNC_000009.11:g.191
    72898_19248426inv
    GRCh37.p13First PassNC_000009.11Chr919,172,89819,248,426

    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)
    nssv187857931.1e-053275818
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