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nsv7044511

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,503

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 17 studies. See in: genome view    
    Submitted genomic134,400,640-134,406,142Question Mark
    Overlapping variant regions from other studies: 97 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):133,736,331-133,741,833Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044511Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5134,400,640134,406,142
    nsv7044511RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5133,736,331133,741,833

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18775361inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18775361Submitted genomicNC_000005.10:g.134
    400640_134406142in
    v
    GRCh38 (hg38)NC_000005.10Chr5134,400,640134,406,142
    nssv18775361RemappedPerfectNC_000005.9:g.1337
    36331_133741833inv
    GRCh37.p13First PassNC_000005.9Chr5133,736,331133,741,833

    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)
    nssv187753614e-061276268
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