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nsv7070719

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,725

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 31 studies. See in: genome view    
    Submitted genomic36,245,720-36,251,444Question Mark
    Overlapping variant regions from other studies: 146 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):36,736,622-36,742,346Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7070719Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,245,72036,251,444
    nsv7070719RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,736,62236,742,346

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758590inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758590Submitted genomicNC_000019.10:g.362
    45720_36251444inv
    GRCh38 (hg38)NC_000019.10Chr1936,245,72036,251,444
    nssv18758590RemappedPerfectNC_000019.9:g.3673
    6622_36742346inv
    GRCh37.p13First PassNC_000019.9Chr1936,736,62236,742,346

    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)
    nssv187585901.8e-054272664
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