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nsv6511441

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,225

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 157 SVs from 34 studies. See in: genome view    
    Submitted genomic69,705,529-69,714,753Question Mark
    Overlapping variant regions from other studies: 157 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):69,739,432-69,748,656Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6511441Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1669,705,52969,714,753
    nsv6511441RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1669,739,43269,748,656

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18031231deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18031231Submitted genomicNC_000016.10:g.697
    05529_69714753del
    GRCh38 (hg38)NC_000016.10Chr1669,705,52969,714,753
    nssv18031231RemappedPerfectNC_000016.9:g.6973
    9432_69748656del
    GRCh37.p13First PassNC_000016.9Chr1669,739,43269,748,656

    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)
    nssv18031231<0.001139278
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