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nsv6505870

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 12 studies. See in: genome view    
    Submitted genomic48,197,401-48,198,800Question Mark
    Overlapping variant regions from other studies: 97 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):48,489,598-48,490,997Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6505870Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1548,197,40148,198,800
    nsv6505870RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1548,489,59848,490,997

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18024720deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18024720Submitted genomicNC_000015.10:g.481
    97401_48198800del
    GRCh38 (hg38)NC_000015.10Chr1548,197,40148,198,800
    nssv18024720RemappedPerfectNC_000015.9:g.4848
    9598_48490997del
    GRCh37.p13First PassNC_000015.9Chr1548,489,59848,490,997

    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)
    nssv18024720<0.001138824
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