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nsv6963368

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,840

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 239 SVs from 50 studies. See in: genome view    
    Submitted genomic3,047,735-3,058,574Question Mark
    Overlapping variant regions from other studies: 239 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):3,097,736-3,108,575Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6963368Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr163,047,7353,058,574
    nsv6963368RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr163,097,7363,108,575

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18398997deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18398997Submitted genomicNC_000016.10:g.304
    7735_3058574del
    GRCh38 (hg38)NC_000016.10Chr163,047,7353,058,574
    nssv18398997RemappedPerfectNC_000016.9:g.3097
    736_3108575del
    GRCh37.p13First PassNC_000016.9Chr163,097,7363,108,575

    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)
    nssv183989971.1e-053276218
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