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nsv6551425

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:561

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 17 studies. See in: genome view    
    Submitted genomic203,767,513-203,768,073Question Mark
    Overlapping variant regions from other studies: 114 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):203,736,641-203,737,201Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6551425Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1203,767,513203,768,073
    nsv6551425RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1203,736,641203,737,201

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248941inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248941Submitted genomicNC_000001.11:g.203
    767513_203768073in
    v
    GRCh38 (hg38)NC_000001.11Chr1203,767,513203,768,073
    nssv18248941RemappedPerfectNC_000001.10:g.203
    736641_203737201in
    v
    GRCh37.p13First PassNC_000001.10Chr1203,736,641203,737,201

    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)
    nssv18248941<0.001134860
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