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nsv7001253

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:179

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 22 studies. See in: genome view    
    Submitted genomic38,813,072-38,813,250Question Mark
    Overlapping variant regions from other studies: 125 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):39,303,712-39,303,890Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7001253Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1938,813,07238,813,250
    nsv7001253RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1939,303,71239,303,890

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18635831duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18635831Submitted genomicNC_000019.10:g.388
    13072_38813250dup
    GRCh38 (hg38)NC_000019.10Chr1938,813,07238,813,250
    nssv18635831RemappedPerfectNC_000019.9:g.3930
    3712_39303890dup
    GRCh37.p13First PassNC_000019.9Chr1939,303,71239,303,890

    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)
    nssv186358319e-062227926
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