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nsv6790182

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:232,313

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 558 SVs from 50 studies. See in: genome view    
    Submitted genomic131,697,382-131,929,694Question Mark
    Overlapping variant regions from other studies: 558 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):131,033,075-131,265,387Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6790182Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5131,697,382131,929,694
    nsv6790182RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5131,033,075131,265,387

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18508234deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18508234Submitted genomicNC_000005.10:g.131
    697382_131929694de
    l
    GRCh38 (hg38)NC_000005.10Chr5131,697,382131,929,694
    nssv18508234RemappedPerfectNC_000005.9:g.1310
    33075_131265387del
    GRCh37.p13First PassNC_000005.9Chr5131,033,075131,265,387

    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)
    nssv185082344e-061276084
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