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nsv6657884

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,745

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 40 studies. See in: genome view    
    Submitted genomic99,095,980-99,115,724Question Mark
    Overlapping variant regions from other studies: 174 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):99,561,536-99,581,280Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6657884Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr199,095,98099,115,724
    nsv6657884RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr199,561,53699,581,280

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18641104duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18641104Submitted genomicNC_000001.11:g.990
    95980_99115724dup
    GRCh38 (hg38)NC_000001.11Chr199,095,98099,115,724
    nssv18641104RemappedPerfectNC_000001.10:g.995
    61536_99581280dup
    GRCh37.p13First PassNC_000001.10Chr199,561,53699,581,280

    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)
    nssv186411044e-061275492
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