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nsv6359678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:484

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 26 studies. See in: genome view    
    Submitted genomic15,799,557-15,800,040Question Mark
    Overlapping variant regions from other studies: 145 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):15,801,180-15,801,663Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6359678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr415,799,55715,800,040
    nsv6359678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr415,801,18015,801,663

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18111088deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18111088Submitted genomicNC_000004.12:g.157
    99557_15800040del
    GRCh38 (hg38)NC_000004.12Chr415,799,55715,800,040
    nssv18111088RemappedPerfectNC_000004.11:g.158
    01180_15801663del
    GRCh37.p13First PassNC_000004.11Chr415,801,18015,801,663

    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)
    nssv18111088<0.0012338022
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