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nsv6973607

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:173,732

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1089 SVs from 83 studies. See in: genome view    
    Submitted genomic104,978,362-105,152,093Question Mark
    Overlapping variant regions from other studies: 1069 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):105,444,699-105,618,430Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6973607Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14104,978,362105,152,093
    nsv6973607RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14105,444,699105,618,430

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611207duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611207Submitted genomicNC_000014.9:g.1049
    78362_105152093dup
    GRCh38 (hg38)NC_000014.9Chr14104,978,362105,152,093
    nssv18611207RemappedPerfectNC_000014.8:g.1054
    44699_105618430dup
    GRCh37.p13First PassNC_000014.8Chr14105,444,699105,618,430

    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)
    nssv186112071.8e-055275316
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