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nsv6675874

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:717,297

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1572 SVs from 74 studies. See in: genome view    
    Submitted genomic232,900,608-233,617,904Question Mark
    Overlapping variant regions from other studies: 1575 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):233,036,354-233,753,650Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6675874Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1232,900,608233,617,904
    nsv6675874RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1233,036,354233,753,650

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18609295duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18609295Submitted genomicNC_000001.11:g.232
    900608_233617904du
    p
    GRCh38 (hg38)NC_000001.11Chr1232,900,608233,617,904
    nssv18609295RemappedPerfectNC_000001.10:g.233
    036354_233753650du
    p
    GRCh37.p13First PassNC_000001.10Chr1233,036,354233,753,650

    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)
    nssv186092954e-061275830
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