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nsv6675008

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 135 SVs from 20 studies. See in: genome view    
    Submitted genomic233,624,901-233,630,500Question Mark
    Overlapping variant regions from other studies: 138 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):233,760,647-233,766,246Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6675008Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1233,624,901233,630,500
    nsv6675008RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1233,760,647233,766,246

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370289deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370289Submitted genomicNC_000001.11:g.233
    624901_233630500de
    l
    GRCh38 (hg38)NC_000001.11Chr1233,624,901233,630,500
    nssv18370289RemappedPerfectNC_000001.10:g.233
    760647_233766246de
    l
    GRCh37.p13First PassNC_000001.10Chr1233,760,647233,766,246

    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)
    nssv183702894e-061276108
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