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nsv6525329

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 39 studies. See in: genome view    
    Submitted genomic49,944,901-49,950,000Question Mark
    Overlapping variant regions from other studies: 158 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):50,448,158-50,453,257Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6525329Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1949,944,90149,950,000
    nsv6525329RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1950,448,15850,453,257

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049063deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049063Submitted genomicNC_000019.10:g.499
    44901_49950000del
    GRCh38 (hg38)NC_000019.10Chr1949,944,90149,950,000
    nssv18049063RemappedPerfectNC_000019.9:g.5044
    8158_50453257del
    GRCh37.p13First PassNC_000019.9Chr1950,448,15850,453,257

    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)
    nssv180490630.0014339198
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