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nsv6738454

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:194,282

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 687 SVs from 53 studies. See in: genome view    
    Submitted genomic147,627,505-147,821,786Question Mark
    Overlapping variant regions from other studies: 687 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):148,548,656-148,742,937Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6738454Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4147,627,505147,821,786
    nsv6738454RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4148,548,656148,742,937

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18685964duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18685964Submitted genomicNC_000004.12:g.147
    627505_147821786du
    p
    GRCh38 (hg38)NC_000004.12Chr4147,627,505147,821,786
    nssv18685964RemappedPerfectNC_000004.11:g.148
    548656_148742937du
    p
    GRCh37.p13First PassNC_000004.11Chr4148,548,656148,742,937

    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)
    nssv186859644e-061275442
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