U.S. flag

An official website of the United States government

nsv6486468

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:146,282

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 367 SVs from 50 studies. See in: genome view    
    Submitted genomic60,936,510-61,082,791Question Mark
    Overlapping variant regions from other studies: 367 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):61,403,228-61,549,509Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6486468Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1460,936,51061,082,791
    nsv6486468RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1461,403,22861,549,509

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18020333deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18020333Submitted genomicNC_000014.9:g.6093
    6510_61082791del
    GRCh38 (hg38)NC_000014.9Chr1460,936,51061,082,791
    nssv18020333RemappedPerfectNC_000014.8:g.6140
    3228_61549509del
    GRCh37.p13First PassNC_000014.8Chr1461,403,22861,549,509

    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)
    nssv18020333<0.001139086
    Support Center