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nsv7055525

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,510

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 191 SVs from 40 studies. See in: genome view    
    Submitted genomic20,166,851-20,188,360Question Mark
    Overlapping variant regions from other studies: 191 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):20,167,082-20,188,591Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055525Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr620,166,85120,188,360
    nsv7055525RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr620,167,08220,188,591

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777384inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777384Submitted genomicNC_000006.12:g.201
    66851_20188360inv
    GRCh38 (hg38)NC_000006.12Chr620,166,85120,188,360
    nssv18777384RemappedPerfectNC_000006.11:g.201
    67082_20188591inv
    GRCh37.p13First PassNC_000006.11Chr620,167,08220,188,591

    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)
    nssv187773844e-061276268
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