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nsv7139680

  • 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: 79 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):21,501,132-21,501,132Question Mark
    Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
    Submitted genomic21,969,274-21,969,274Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7139680RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1421,501,13221,501,132
    nsv7139680Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1421,969,27421,969,274

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18833473insertionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18833473RemappedPerfectNC_000014.9:g.2150
    1132_21501133ins56
    GRCh38.p12First PassNC_000014.9Chr1421,501,13221,501,132
    nssv18833473Submitted genomicNC_000014.8:g.2196
    9274_21969275ins56
    GRCh37.p13NC_000014.8Chr1421,969,27421,969,274

    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)
    nssv188334730.512
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