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nsv6663848

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:454,219

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1993 SVs from 93 studies. See in: genome view    
    Submitted genomic247,940,888-248,395,106Question Mark
    Overlapping variant regions from other studies: 1996 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):248,104,190-248,558,407Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6663848Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1247,940,888248,395,106
    nsv6663848RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1248,104,190248,558,407

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609892duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609892Submitted genomicNC_000001.11:g.247
    940888_248395106du
    p
    GRCh38 (hg38)NC_000001.11Chr1247,940,888248,395,106
    nssv18609892RemappedPerfectNC_000001.10:g.248
    104190_248558407du
    p
    GRCh37.p13First PassNC_000001.10Chr1248,104,190248,558,407

    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)
    nssv186098924e-061274188
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