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nsv6364971

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 19 studies. See in: genome view    
    Submitted genomic157,587,101-157,589,000Question Mark
    Overlapping variant regions from other studies: 111 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):157,304,890-157,306,789Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6364971Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3157,587,101157,589,000
    nsv6364971RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3157,304,890157,306,789

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18096538deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18096538Submitted genomicNC_000003.12:g.157
    587101_157589000de
    l
    GRCh38 (hg38)NC_000003.12Chr3157,587,101157,589,000
    nssv18096538RemappedPerfectNC_000003.11:g.157
    304890_157306789de
    l
    GRCh37.p13First PassNC_000003.11Chr3157,304,890157,306,789

    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)
    nssv18096538<0.001138450
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