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nsv7077675

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:97,376

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 534 SVs from 57 studies. See in: genome view    
    Submitted genomic43,438,575-43,535,950Question Mark
    Overlapping variant regions from other studies: 534 SVs from 57 studies. See in: genome view    
    Remapped(Score: Perfect):43,942,727-44,040,102Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077675Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1943,438,57543,535,950
    nsv7077675RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1943,942,72744,040,102

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760773inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760773Submitted genomicNC_000019.10:g.434
    38575_43535950inv
    GRCh38 (hg38)NC_000019.10Chr1943,438,57543,535,950
    nssv18760773RemappedPerfectNC_000019.9:g.4394
    2727_44040102inv
    GRCh37.p13First PassNC_000019.9Chr1943,942,72744,040,102

    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)
    nssv187607737e-062275068
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