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nsv7010621

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:42,740

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 388 SVs from 50 studies. See in: genome view    
    Submitted genomic18,240,453-18,283,192Question Mark
    Overlapping variant regions from other studies: 388 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):18,351,263-18,394,002Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7010621Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1918,240,45318,283,192
    nsv7010621RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1918,351,26318,394,002

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639381duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639381Submitted genomicNC_000019.10:g.182
    40453_18283192dup
    GRCh38 (hg38)NC_000019.10Chr1918,240,45318,283,192
    nssv18639381RemappedPerfectNC_000019.9:g.1835
    1263_18394002dup
    GRCh37.p13First PassNC_000019.9Chr1918,351,26318,394,002

    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)
    nssv186393814e-061275660
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