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nsv7061767

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:128,032

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2753 SVs from 94 studies. See in: genome view    
    Submitted genomic105,547,482-105,675,513Question Mark
    Overlapping variant regions from other studies: 2736 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):106,013,819-106,141,850Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061767Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14105,547,482105,675,513
    nsv7061767RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14106,013,819106,141,850

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754215inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754215Submitted genomicNC_000014.9:g.1055
    47482_105675513inv
    GRCh38 (hg38)NC_000014.9Chr14105,547,482105,675,513
    nssv18754215RemappedPerfectNC_000014.8:g.1060
    13819_106141850inv
    GRCh37.p13First PassNC_000014.8Chr14106,013,819106,141,850

    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)
    nssv187542154e-061276268
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