U.S. flag

An official website of the United States government

nsv7046897

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,366,224

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4574 SVs from 100 studies. See in: genome view    
    Submitted genomic244,176,149-245,542,372Question Mark
    Overlapping variant regions from other studies: 4577 SVs from 100 studies. See in: genome view    
    Remapped(Score: Perfect):244,339,451-245,705,674Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046897Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1244,176,149245,542,372
    nsv7046897RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1244,339,451245,705,674

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759448inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759448Submitted genomicNC_000001.11:g.244
    176149_245542372in
    v
    GRCh38 (hg38)NC_000001.11Chr1244,176,149245,542,372
    nssv18759448RemappedPerfectNC_000001.10:g.244
    339451_245705674in
    v
    GRCh37.p13First PassNC_000001.10Chr1244,339,451245,705,674

    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)
    nssv187594484e-061276268
    Support Center