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nsv7074285

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,254,846

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10909 SVs from 125 studies. See in: genome view    
    Submitted genomic25,121,393-29,376,238Question Mark
    Overlapping variant regions from other studies: 10911 SVs from 125 studies. See in: genome view    
    Remapped(Score: Perfect):25,142,939-29,397,785Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7074285Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1125,121,39329,376,238
    nsv7074285RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1125,142,93929,397,785

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749583inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749583Submitted genomicNC_000011.10:g.251
    21393_29376238inv
    GRCh38 (hg38)NC_000011.10Chr1125,121,39329,376,238
    nssv18749583RemappedPerfectNC_000011.9:g.2514
    2939_29397785inv
    GRCh37.p13First PassNC_000011.9Chr1125,142,93929,397,785

    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)
    nssv187495834e-061276268
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