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nsv7051977

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,626

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 25 studies. See in: genome view    
    Submitted genomic80,266,608-80,271,233Question Mark
    Overlapping variant regions from other studies: 135 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):81,187,762-81,192,387Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051977Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr480,266,60880,271,233
    nsv7051977RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr481,187,76281,192,387

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776344inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776344Submitted genomicNC_000004.12:g.802
    66608_80271233inv
    GRCh38 (hg38)NC_000004.12Chr480,266,60880,271,233
    nssv18776344RemappedPerfectNC_000004.11:g.811
    87762_81192387inv
    GRCh37.p13First PassNC_000004.11Chr481,187,76281,192,387

    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)
    nssv187763447e-062275430
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