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nsv6886722

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:70,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 336 SVs from 59 studies. See in: genome view    
    Submitted genomic97,320,001-97,390,200Question Mark
    Overlapping variant regions from other studies: 336 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):99,079,758-99,149,957Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6886722Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1097,320,00197,390,200
    nsv6886722RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1099,079,75899,149,957

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18579908duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18579908Submitted genomicNC_000010.11:g.973
    20001_97390200dup
    GRCh38 (hg38)NC_000010.11Chr1097,320,00197,390,200
    nssv18579908RemappedPerfectNC_000010.10:g.990
    79758_99149957dup
    GRCh37.p13First PassNC_000010.10Chr1099,079,75899,149,957

    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)
    nssv185799084e-061276028
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