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nsv6957461

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,010,930

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2857 SVs from 105 studies. See in: genome view    
    Submitted genomic42,155,232-43,166,161Question Mark
    Overlapping variant regions from other studies: 2857 SVs from 105 studies. See in: genome view    
    Remapped(Score: Perfect):42,729,368-43,740,297Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6957461Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1342,155,23243,166,161
    nsv6957461RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1342,729,36843,740,297

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18377926deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18377926Submitted genomicNC_000013.11:g.421
    55232_43166161del
    GRCh38 (hg38)NC_000013.11Chr1342,155,23243,166,161
    nssv18377926RemappedPerfectNC_000013.10:g.427
    29368_43740297del
    GRCh37.p13First PassNC_000013.10Chr1342,729,36843,740,297

    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)
    nssv183779264e-061275418
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