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nsv6991648

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:183,553

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 760 SVs from 73 studies. See in: genome view    
    Submitted genomic77,170,437-77,353,989Question Mark
    Overlapping variant regions from other studies: 760 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):77,204,334-77,387,886Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6991648Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1677,170,43777,353,989
    nsv6991648RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1677,204,33477,387,886

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18625308duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18625308Submitted genomicNC_000016.10:g.771
    70437_77353989dup
    GRCh38 (hg38)NC_000016.10Chr1677,170,43777,353,989
    nssv18625308RemappedPerfectNC_000016.9:g.7720
    4334_77387886dup
    GRCh37.p13First PassNC_000016.9Chr1677,204,33477,387,886

    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)
    nssv186253084e-061274602
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