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nsv7007661

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:467

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 29 studies. See in: genome view    
    Submitted genomic17,289,862-17,290,328Question Mark
    Overlapping variant regions from other studies: 128 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):17,400,671-17,401,137Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7007661Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1917,289,86217,290,328
    nsv7007661RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1917,400,67117,401,137

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639320duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639320Submitted genomicNC_000019.10:g.172
    89862_17290328dup
    GRCh38 (hg38)NC_000019.10Chr1917,289,86217,290,328
    nssv18639320RemappedPerfectNC_000019.9:g.1740
    0671_17401137dup
    GRCh37.p13First PassNC_000019.9Chr1917,400,67117,401,137

    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)
    nssv186393204e-061234214
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