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nsv7049375

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:382,982

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 914 SVs from 69 studies. See in: genome view    
    Submitted genomic45,009,134-45,392,115Question Mark
    Overlapping variant regions from other studies: 914 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):45,050,626-45,433,607Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7049375Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr345,009,13445,392,115
    nsv7049375RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr345,050,62645,433,607

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771314inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771314Submitted genomicNC_000003.12:g.450
    09134_45392115inv
    GRCh38 (hg38)NC_000003.12Chr345,009,13445,392,115
    nssv18771314RemappedPerfectNC_000003.11:g.450
    50626_45433607inv
    GRCh37.p13First PassNC_000003.11Chr345,050,62645,433,607

    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)
    nssv187713144e-061276268
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