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nsv7077440

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,272,327

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17786 SVs from 112 studies. See in: genome view    
    Submitted genomic95,324,680-102,597,006Question Mark
    Overlapping variant regions from other studies: 17790 SVs from 112 studies. See in: genome view    
    Remapped(Score: Good):95,976,934-103,249,356Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077440Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1395,324,680102,597,006
    nsv7077440RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1395,976,934103,249,356

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754908inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754908Submitted genomicNC_000013.11:g.953
    24680_102597006inv
    GRCh38 (hg38)NC_000013.11Chr1395,324,680102,597,006
    nssv18754908RemappedGoodNC_000013.10:g.959
    76934_103249356inv
    GRCh37.p13First PassNC_000013.10Chr1395,976,934103,249,356

    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)
    nssv187549084e-061276266
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