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nsv6356569

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,834

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 32 studies. See in: genome view    
    Submitted genomic101,969,464-101,980,297Question Mark
    Overlapping variant regions from other studies: 120 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):101,688,308-101,699,141Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6356569Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3101,969,464101,980,297
    nsv6356569RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3101,688,308101,699,141

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18092434deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18092434Submitted genomicNC_000003.12:g.101
    969464_101980297de
    l
    GRCh38 (hg38)NC_000003.12Chr3101,969,464101,980,297
    nssv18092434RemappedPerfectNC_000003.11:g.101
    688308_101699141de
    l
    GRCh37.p13First PassNC_000003.11Chr3101,688,308101,699,141

    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)
    nssv18092434<0.001139162
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