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nsv7053695

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,357

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 127 SVs from 25 studies. See in: genome view    
    Submitted genomic44,514,581-44,518,937Question Mark
    Overlapping variant regions from other studies: 127 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):44,980,253-44,984,609Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053695Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr144,514,58144,518,937
    nsv7053695RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr144,980,25344,984,609

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761006inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761006Submitted genomicNC_000001.11:g.445
    14581_44518937inv
    GRCh38 (hg38)NC_000001.11Chr144,514,58144,518,937
    nssv18761006RemappedPerfectNC_000001.10:g.449
    80253_44984609inv
    GRCh37.p13First PassNC_000001.10Chr144,980,25344,984,609

    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)
    nssv187610064e-061276268
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