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nsv7071053

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,857

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 232 SVs from 44 studies. See in: genome view    
    Submitted genomic79,556,685-79,614,541Question Mark
    Overlapping variant regions from other studies: 246 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):81,316,441-81,374,297Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7071053Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1079,556,68579,614,541
    nsv7071053RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1081,316,44181,374,297

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18738947inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18738947Submitted genomicNC_000010.11:g.795
    56685_79614541inv
    GRCh38 (hg38)NC_000010.11Chr1079,556,68579,614,541
    nssv18738947RemappedPerfectNC_000010.10:g.813
    16441_81374297inv
    GRCh37.p13First PassNC_000010.10Chr1081,316,44181,374,297

    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)
    nssv187389470.40697835239352
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