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nsv7003570

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:151,230

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 520 SVs from 53 studies. See in: genome view    
    Submitted genomic50,884,950-51,036,179Question Mark
    Overlapping variant regions from other studies: 520 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):48,411,320-48,562,549Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7003570Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1850,884,95051,036,179
    nsv7003570RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1848,411,32048,562,549

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18417687deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18417687Submitted genomicNC_000018.10:g.508
    84950_51036179del
    GRCh38 (hg38)NC_000018.10Chr1850,884,95051,036,179
    nssv18417687RemappedPerfectNC_000018.9:g.4841
    1320_48562549del
    GRCh37.p13First PassNC_000018.9Chr1848,411,32048,562,549

    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)
    nssv184176874e-061275674
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