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nsv6750652

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,556

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 123 SVs from 31 studies. See in: genome view    
    Submitted genomic119,298,780-119,300,335Question Mark
    Overlapping variant regions from other studies: 123 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):120,219,935-120,221,490Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6750652Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4119,298,780119,300,335
    nsv6750652RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4120,219,935120,221,490

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18487035deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18487035Submitted genomicNC_000004.12:g.119
    298780_119300335de
    l
    GRCh38 (hg38)NC_000004.12Chr4119,298,780119,300,335
    nssv18487035RemappedPerfectNC_000004.11:g.120
    219935_120221490de
    l
    GRCh37.p13First PassNC_000004.11Chr4120,219,935120,221,490

    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)
    nssv184870357e-062272888
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