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nsv6663483

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:426

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 25 studies. See in: genome view    
    Submitted genomic219,935,074-219,935,499Question Mark
    Overlapping variant regions from other studies: 155 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):220,108,416-220,108,841Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6663483Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1219,935,074219,935,499
    nsv6663483RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1220,108,416220,108,841

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18607210duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18607210Submitted genomicNC_000001.11:g.219
    935074_219935499du
    p
    GRCh38 (hg38)NC_000001.11Chr1219,935,074219,935,499
    nssv18607210RemappedPerfectNC_000001.10:g.220
    108416_220108841du
    p
    GRCh37.p13First PassNC_000001.10Chr1220,108,416220,108,841

    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)
    nssv186072102.4e-056243992
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