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nsv6683744

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:232,267

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 648 SVs from 65 studies. See in: genome view    
    Submitted genomic78,047,809-78,280,075Question Mark
    Overlapping variant regions from other studies: 648 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):78,274,935-78,507,201Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6683744Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr278,047,80978,280,075
    nsv6683744RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr278,274,93578,507,201

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18468706deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18468706Submitted genomicNC_000002.12:g.780
    47809_78280075del
    GRCh38 (hg38)NC_000002.12Chr278,047,80978,280,075
    nssv18468706RemappedPerfectNC_000002.11:g.782
    74935_78507201del
    GRCh37.p13First PassNC_000002.11Chr278,274,93578,507,201

    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)
    nssv184687064e-061272550
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