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nsv6501688

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,737

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 15 studies. See in: genome view    
    Submitted genomic43,295,452-43,297,188Question Mark
    Overlapping variant regions from other studies: 108 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):43,587,650-43,589,386Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6501688Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1543,295,45243,297,188
    nsv6501688RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1543,587,65043,589,386

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18023979deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18023979Submitted genomicNC_000015.10:g.432
    95452_43297188del
    GRCh38 (hg38)NC_000015.10Chr1543,295,45243,297,188
    nssv18023979RemappedPerfectNC_000015.9:g.4358
    7650_43589386del
    GRCh37.p13First PassNC_000015.9Chr1543,587,65043,589,386

    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)
    nssv18023979<0.001538640
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