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nsv6980328

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 188 SVs from 28 studies. See in: genome view    
    Submitted genomic43,854,001-43,871,500Question Mark
    Overlapping variant regions from other studies: 186 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):41,931,369-41,948,868Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6980328Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1743,854,00143,871,500
    nsv6980328RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1741,931,36941,948,868

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18627573duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18627573Submitted genomicNC_000017.11:g.438
    54001_43871500dup
    GRCh38 (hg38)NC_000017.11Chr1743,854,00143,871,500
    nssv18627573RemappedPerfectNC_000017.10:g.419
    31369_41948868dup
    GRCh37.p13First PassNC_000017.10Chr1741,931,36941,948,868

    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)
    nssv186275734e-061275520
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