U.S. flag

An official website of the United States government

nsv7057605

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,825,369

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17973 SVs from 117 studies. See in: genome view    
    Submitted genomic78,336,704-86,162,072Question Mark
    Overlapping variant regions from other studies: 17973 SVs from 117 studies. See in: genome view    
    Remapped(Score: Perfect):78,802,388-86,627,755Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7057605Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr178,336,70486,162,072
    nsv7057605RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr178,802,38886,627,755

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762504inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762504Submitted genomicNC_000001.11:g.783
    36704_86162072inv
    GRCh38 (hg38)NC_000001.11Chr178,336,70486,162,072
    nssv18762504RemappedPerfectNC_000001.10:g.788
    02388_86627755inv
    GRCh37.p13First PassNC_000001.10Chr178,802,38886,627,755

    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)
    nssv187625041.8e-055276214
    Support Center