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nsv6708557

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,285

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 47 studies. See in: genome view    
    Submitted genomic11,733,413-11,741,697Question Mark
    Overlapping variant regions from other studies: 173 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):11,774,887-11,783,171Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6708557Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr311,733,41311,741,697
    nsv6708557RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr311,774,88711,783,171

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18472789deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18472789Submitted genomicNC_000003.12:g.117
    33413_11741697del
    GRCh38 (hg38)NC_000003.12Chr311,733,41311,741,697
    nssv18472789RemappedPerfectNC_000003.11:g.117
    74887_11783171del
    GRCh37.p13First PassNC_000003.11Chr311,774,88711,783,171

    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)
    nssv184727891.8e-055275910
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