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nsv6978422

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,172

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 351 SVs from 52 studies. See in: genome view    
    Submitted genomic75,423,467-75,460,638Question Mark
    Overlapping variant regions from other studies: 351 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):73,419,548-73,456,719Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6978422Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1775,423,46775,460,638
    nsv6978422RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1773,419,54873,456,719

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631282duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631282Submitted genomicNC_000017.11:g.754
    23467_75460638dup
    GRCh38 (hg38)NC_000017.11Chr1775,423,46775,460,638
    nssv18631282RemappedPerfectNC_000017.10:g.734
    19548_73456719dup
    GRCh37.p13First PassNC_000017.10Chr1773,419,54873,456,719

    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)
    nssv186312824e-061274528
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