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nsv7040230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,028

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
    Submitted genomic14,972,465-14,977,492Question Mark
    Overlapping variant regions from other studies: 136 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):14,974,089-14,979,116Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7040230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr414,972,46514,977,492
    nsv7040230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr414,974,08914,979,116

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18772693inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18772693Submitted genomicNC_000004.12:g.149
    72465_14977492inv
    GRCh38 (hg38)NC_000004.12Chr414,972,46514,977,492
    nssv18772693RemappedPerfectNC_000004.11:g.149
    74089_14979116inv
    GRCh37.p13First PassNC_000004.11Chr414,974,08914,979,116

    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)
    nssv187726934e-061276268
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