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nsv6800555

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83,458

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 650 SVs from 67 studies. See in: genome view    
    Submitted genomic159,658,014-159,741,471Question Mark
    Overlapping variant regions from other studies: 650 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):160,079,046-160,162,503Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6800555Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6159,658,014159,741,471
    nsv6800555RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,079,046160,162,503

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18713265duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18713265Submitted genomicNC_000006.12:g.159
    658014_159741471du
    p
    GRCh38 (hg38)NC_000006.12Chr6159,658,014159,741,471
    nssv18713265RemappedPerfectNC_000006.11:g.160
    079046_160162503du
    p
    GRCh37.p13First PassNC_000006.11Chr6160,079,046160,162,503

    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)
    nssv187132654e-061272020
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