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nsv7045537

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,924,905

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5955 SVs from 110 studies. See in: genome view    
    Submitted genomic33,552,668-35,477,572Question Mark
    Overlapping variant regions from other studies: 5955 SVs from 110 studies. See in: genome view    
    Remapped(Score: Perfect):33,554,290-35,479,194Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045537Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr433,552,66835,477,572
    nsv7045537RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr433,554,29035,479,194

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773505inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773505Submitted genomicNC_000004.12:g.335
    52668_35477572inv
    GRCh38 (hg38)NC_000004.12Chr433,552,66835,477,572
    nssv18773505RemappedPerfectNC_000004.11:g.335
    54290_35479194inv
    GRCh37.p13First PassNC_000004.11Chr433,554,29035,479,194

    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)
    nssv187735053.2e-059274590
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