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nsv7068052

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,139,977

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3227 SVs from 92 studies. See in: genome view    
    Submitted genomic93,353,824-94,493,800Question Mark
    Overlapping variant regions from other studies: 3227 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):93,897,053-95,037,029Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068052Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1593,353,82494,493,800
    nsv7068052RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1593,897,05395,037,029

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756679inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756679Submitted genomicNC_000015.10:g.933
    53824_94493800inv
    GRCh38 (hg38)NC_000015.10Chr1593,353,82494,493,800
    nssv18756679RemappedPerfectNC_000015.9:g.9389
    7053_95037029inv
    GRCh37.p13First PassNC_000015.9Chr1593,897,05395,037,029

    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)
    nssv187566794e-061276268
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