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nsv7143702

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

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 94 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):14,274,483-14,274,483Question Mark
    Overlapping variant regions from other studies: 94 SVs from 17 studies. See in: genome view    
    Submitted genomic14,414,607-14,414,607Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7143702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr214,274,48314,274,483
    nsv7143702Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr214,414,60714,414,607

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18837496insertionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18837496RemappedPerfectNC_000002.12:g.142
    74483_14274484ins1
    15
    GRCh38.p12First PassNC_000002.12Chr214,274,48314,274,483
    nssv18837496Submitted genomicNC_000002.11:g.144
    14607_14414608ins1
    15
    GRCh37.p13NC_000002.11Chr214,414,60714,414,607

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv188374960.524
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