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nsv6917626

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 58 SVs from 21 studies. See in: genome view    
    Submitted genomic10,387,538-10,387,719Question Mark
    Overlapping variant regions from other studies: 58 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):10,409,085-10,409,266Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6917626Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1110,387,53810,387,719
    nsv6917626RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1110,409,08510,409,266

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18590569duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18590569Submitted genomicNC_000011.10:g.103
    87538_10387719dup
    GRCh38 (hg38)NC_000011.10Chr1110,387,53810,387,719
    nssv18590569RemappedPerfectNC_000011.9:g.1040
    9085_10409266dup
    GRCh37.p13First PassNC_000011.9Chr1110,409,08510,409,266

    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)
    nssv185905694e-061235100
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