U.S. flag

An official website of the United States government

nsv6534202

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,496

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 34 studies. See in: genome view    
    Submitted genomic57,928,812-57,933,307Question Mark
    Overlapping variant regions from other studies: 110 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):58,440,180-58,444,675Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6534202Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1957,928,81257,933,307
    nsv6534202RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1958,440,18058,444,675

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049012deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049012Submitted genomicNC_000019.10:g.579
    28812_57933307del
    GRCh38 (hg38)NC_000019.10Chr1957,928,81257,933,307
    nssv18049012RemappedPerfectNC_000019.9:g.5844
    0180_58444675del
    GRCh37.p13First PassNC_000019.9Chr1958,440,18058,444,675

    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)
    nssv18049012<0.001238790
    Support Center