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nsv6984488

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 533 SVs from 63 studies. See in: genome view    
    Submitted genomic82,036,901-82,098,400Question Mark
    Overlapping variant regions from other studies: 533 SVs from 63 studies. See in: genome view    
    Remapped(Score: Perfect):79,994,777-80,056,276Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6984488Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1782,036,90182,098,400
    nsv6984488RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1779,994,77780,056,276

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18631577duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18631577Submitted genomicNC_000017.11:g.820
    36901_82098400dup
    GRCh38 (hg38)NC_000017.11Chr1782,036,90182,098,400
    nssv18631577RemappedPerfectNC_000017.10:g.799
    94777_80056276dup
    GRCh37.p13First PassNC_000017.10Chr1779,994,77780,056,276

    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)
    nssv186315775.6e-0515263356
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