U.S. flag

An official website of the United States government

nsv6660969

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:100,656

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 706 SVs from 77 studies. See in: genome view    
    Submitted genomic247,944,356-248,045,011Question Mark
    Overlapping variant regions from other studies: 709 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):248,107,658-248,208,313Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6660969Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1247,944,356248,045,011
    nsv6660969RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1248,107,658248,208,313

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609893duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609893Submitted genomicNC_000001.11:g.247
    944356_248045011du
    p
    GRCh38 (hg38)NC_000001.11Chr1247,944,356248,045,011
    nssv18609893RemappedPerfectNC_000001.10:g.248
    107658_248208313du
    p
    GRCh37.p13First PassNC_000001.10Chr1248,107,658248,208,313

    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)
    nssv186098934e-061275000
    Support Center