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nsv6792778

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:120

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 58 SVs from 13 studies. See in: genome view    
    Submitted genomic175,697,703-175,697,822Question Mark
    Overlapping variant regions from other studies: 58 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):175,124,706-175,124,825Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6792778Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5175,697,703175,697,822
    nsv6792778RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5175,124,706175,124,825

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18699338duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18699338Submitted genomicNC_000005.10:g.175
    697703_175697822du
    p
    GRCh38 (hg38)NC_000005.10Chr5175,697,703175,697,822
    nssv18699338RemappedPerfectNC_000005.9:g.1751
    24706_175124825dup
    GRCh37.p13First PassNC_000005.9Chr5175,124,706175,124,825

    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)
    nssv186993381.3e-053230594
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