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nsv7056364

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:145,581

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 661 SVs from 55 studies. See in: genome view    
    Submitted genomic245,311,621-245,457,201Question Mark
    Overlapping variant regions from other studies: 664 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):245,474,923-245,620,503Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056364Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1245,311,621245,457,201
    nsv7056364RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1245,474,923245,620,503

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759464inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759464Submitted genomicNC_000001.11:g.245
    311621_245457201in
    v
    GRCh38 (hg38)NC_000001.11Chr1245,311,621245,457,201
    nssv18759464RemappedPerfectNC_000001.10:g.245
    474923_245620503in
    v
    GRCh37.p13First PassNC_000001.10Chr1245,474,923245,620,503

    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)
    nssv18759464<0.001110269510
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