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nsv7071248

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:421,987

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1333 SVs from 84 studies. See in: genome view    
    Submitted genomic52,189,470-52,611,456Question Mark
    Overlapping variant regions from other studies: 1333 SVs from 84 studies. See in: genome view    
    Remapped(Score: Perfect):52,763,605-53,185,591Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7071248Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1352,189,47052,611,456
    nsv7071248RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,763,60553,185,591

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18752994inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18752994Submitted genomicNC_000013.11:g.521
    89470_52611456inv
    GRCh38 (hg38)NC_000013.11Chr1352,189,47052,611,456
    nssv18752994RemappedPerfectNC_000013.10:g.527
    63605_53185591inv
    GRCh37.p13First PassNC_000013.10Chr1352,763,60553,185,591

    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)
    nssv187529944e-061276268
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