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nsv6644714

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,934

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 166 SVs from 32 studies. See in: genome view    
    Submitted genomic172,420,186-172,427,119Question Mark
    Overlapping variant regions from other studies: 169 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):172,389,326-172,396,259Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644714Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1172,420,186172,427,119
    nsv6644714RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1172,389,326172,396,259

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18364026deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18364026Submitted genomicNC_000001.11:g.172
    420186_172427119de
    l
    GRCh38 (hg38)NC_000001.11Chr1172,420,186172,427,119
    nssv18364026RemappedPerfectNC_000001.10:g.172
    389326_172396259de
    l
    GRCh37.p13First PassNC_000001.10Chr1172,389,326172,396,259

    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)
    nssv183640266e-0517276096
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