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nsv6640227

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 452 SVs from 70 studies. See in: genome view    
    Submitted genomic115,653,601-115,739,300Question Mark
    Overlapping variant regions from other studies: 454 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):116,196,222-116,281,921Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6640227Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1115,653,601115,739,300
    nsv6640227RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1116,196,222116,281,921

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18347121deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18347121Submitted genomicNC_000001.11:g.115
    653601_115739300de
    l
    GRCh38 (hg38)NC_000001.11Chr1115,653,601115,739,300
    nssv18347121RemappedPerfectNC_000001.10:g.116
    196222_116281921de
    l
    GRCh37.p13First PassNC_000001.10Chr1116,196,222116,281,921

    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)
    nssv183471214e-061276248
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