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nsv6669727

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,406

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 147 SVs from 26 studies. See in: genome view    
    Submitted genomic228,494,463-228,496,868Question Mark
    Overlapping variant regions from other studies: 150 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):228,682,164-228,684,569Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6669727Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1228,494,463228,496,868
    nsv6669727RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1228,682,164228,684,569

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18368610deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18368610Submitted genomicNC_000001.11:g.228
    494463_228496868de
    l
    GRCh38 (hg38)NC_000001.11Chr1228,494,463228,496,868
    nssv18368610RemappedPerfectNC_000001.10:g.228
    682164_228684569de
    l
    GRCh37.p13First PassNC_000001.10Chr1228,682,164228,684,569

    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)
    nssv183686107e-062275648
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