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nsv6356859

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 101 SVs from 16 studies. See in: genome view    
    Submitted genomic157,567,301-157,567,800Question Mark
    Overlapping variant regions from other studies: 101 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):157,285,090-157,285,589Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6356859Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3157,567,301157,567,800
    nsv6356859RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3157,285,090157,285,589

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18096536deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18096536Submitted genomicNC_000003.12:g.157
    567301_157567800de
    l
    GRCh38 (hg38)NC_000003.12Chr3157,567,301157,567,800
    nssv18096536RemappedPerfectNC_000003.11:g.157
    285090_157285589de
    l
    GRCh37.p13First PassNC_000003.11Chr3157,285,090157,285,589

    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)
    nssv18096536<0.0012537484
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