U.S. flag

An official website of the United States government

nsv6718054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,390

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 28 studies. See in: genome view    
    Submitted genomic63,853,599-63,861,988Question Mark
    Overlapping variant regions from other studies: 110 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):63,839,275-63,847,664Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6718054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr363,853,59963,861,988
    nsv6718054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr363,839,27563,847,664

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18483742deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18483742Submitted genomicNC_000003.12:g.638
    53599_63861988del
    GRCh38 (hg38)NC_000003.12Chr363,853,59963,861,988
    nssv18483742RemappedPerfectNC_000003.11:g.638
    39275_63847664del
    GRCh37.p13First PassNC_000003.11Chr363,839,27563,847,664

    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)
    nssv184837424e-061276248
    Support Center