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nsv6972145

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 20 studies. See in: genome view    
    Submitted genomic3,451,401-3,455,200Question Mark
    Overlapping variant regions from other studies: 118 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):3,501,401-3,505,200Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6972145Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,451,4013,455,200
    nsv6972145RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,501,4013,505,200

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18402100deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18402100Submitted genomicNC_000016.10:g.345
    1401_3455200del
    GRCh38 (hg38)NC_000016.10Chr163,451,4013,455,200
    nssv18402100RemappedPerfectNC_000016.9:g.3501
    401_3505200del
    GRCh37.p13First PassNC_000016.9Chr163,501,4013,505,200

    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)
    nssv184021004e-061276198
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