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nsv7056279

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,595

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 171 SVs from 34 studies. See in: genome view    
    Submitted genomic77,491,615-77,508,209Question Mark
    Overlapping variant regions from other studies: 171 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):77,957,300-77,973,894Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7056279Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr177,491,61577,508,209
    nsv7056279RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr177,957,30077,973,894

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18762491inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18762491Submitted genomicNC_000001.11:g.774
    91615_77508209inv
    GRCh38 (hg38)NC_000001.11Chr177,491,61577,508,209
    nssv18762491RemappedPerfectNC_000001.10:g.779
    57300_77973894inv
    GRCh37.p13First PassNC_000001.10Chr177,957,30077,973,894

    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)
    nssv187624917e-062276268
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