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nsv6985046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 134 SVs from 20 studies. See in: genome view    
    Submitted genomic79,831,150-79,831,231Question Mark
    Overlapping variant regions from other studies: 133 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):77,804,949-77,805,030Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6985046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1779,831,15079,831,231
    nsv6985046RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1777,804,94977,805,030

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631815duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631815Submitted genomicNC_000017.11:g.798
    31150_79831231dup
    GRCh38 (hg38)NC_000017.11Chr1779,831,15079,831,231
    nssv18631815RemappedPerfectNC_000017.10:g.778
    04949_77805030dup
    GRCh37.p13First PassNC_000017.10Chr1777,804,94977,805,030

    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)
    nssv186318150.005935183254
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