U.S. flag

An official website of the United States government

nsv6597711

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,479,637

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9328 SVs from 106 studies. See in: genome view    
    Submitted genomic55,930,883-58,410,519Question Mark
    Overlapping variant regions from other studies: 9330 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):56,442,249-58,921,886Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6597711Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1955,930,88358,410,519
    nsv6597711RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,442,24958,921,886

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248498inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248498Submitted genomicNC_000019.10:g.559
    30883_58410519inv
    GRCh38 (hg38)NC_000019.10Chr1955,930,88358,410,519
    nssv18248498RemappedPerfectNC_000019.9:g.5644
    2249_58921886inv
    GRCh37.p13First PassNC_000019.9Chr1956,442,24958,921,886

    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)
    nssv182484980.0026231594
    Support Center