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nsv6669454

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:225,824

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 576 SVs from 55 studies. See in: genome view    
    Submitted genomic203,406,944-203,632,767Question Mark
    Overlapping variant regions from other studies: 576 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):203,376,072-203,601,895Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6669454Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1203,406,944203,632,767
    nsv6669454RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1203,376,072203,601,895

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18605784duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18605784Submitted genomicNC_000001.11:g.203
    406944_203632767du
    p
    GRCh38 (hg38)NC_000001.11Chr1203,406,944203,632,767
    nssv18605784RemappedPerfectNC_000001.10:g.203
    376072_203601895du
    p
    GRCh37.p13First PassNC_000001.10Chr1203,376,072203,601,895

    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)
    nssv186057841.8e-051275512
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