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nsv7030335

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 25 studies. See in: genome view    
    Submitted genomic37,395,284-37,395,417Question Mark
    Overlapping variant regions from other studies: 147 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):36,023,687-36,023,820Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7030335Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2037,395,28437,395,417
    nsv7030335RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2036,023,68736,023,820

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18644245duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18644245Submitted genomicNC_000020.11:g.373
    95284_37395417dup
    GRCh38 (hg38)NC_000020.11Chr2037,395,28437,395,417
    nssv18644245RemappedPerfectNC_000020.10:g.360
    23687_36023820dup
    GRCh37.p13First PassNC_000020.10Chr2036,023,68736,023,820

    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)
    nssv186442459e-062215920
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