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nsv6499841

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:397

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 33 studies. See in: genome view    
    Submitted genomic65,326,077-65,326,473Question Mark
    Overlapping variant regions from other studies: 121 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):65,618,415-65,618,811Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6499841Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1565,326,07765,326,473
    nsv6499841RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1565,618,41565,618,811

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18025356deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18025356Submitted genomicNC_000015.10:g.653
    26077_65326473del
    GRCh38 (hg38)NC_000015.10Chr1565,326,07765,326,473
    nssv18025356RemappedPerfectNC_000015.9:g.6561
    8415_65618811del
    GRCh37.p13First PassNC_000015.9Chr1565,618,41565,618,811

    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)
    nssv180253560.036136238308
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