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nsv6728543

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,554

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 230 SVs from 45 studies. See in: genome view    
    Submitted genomic6,592,873-6,611,426Question Mark
    Overlapping variant regions from other studies: 230 SVs from 45 studies. See in: genome view    
    Remapped(Score: Perfect):6,594,600-6,613,153Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6728543Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr46,592,8736,611,426
    nsv6728543RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr46,594,6006,613,153

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18498620deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18498620Submitted genomicNC_000004.12:g.659
    2873_6611426del
    GRCh38 (hg38)NC_000004.12Chr46,592,8736,611,426
    nssv18498620RemappedPerfectNC_000004.11:g.659
    4600_6613153del
    GRCh37.p13First PassNC_000004.11Chr46,594,6006,613,153

    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)
    nssv184986204e-061276246
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