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nsv6601472

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,905

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 31 studies. See in: genome view    
    Submitted genomic99,017,561-99,021,465Question Mark
    Overlapping variant regions from other studies: 113 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):98,615,184-98,619,088Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6601472Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr799,017,56199,021,465
    nsv6601472RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr798,615,18498,619,088

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18161313deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18161313Submitted genomicNC_000007.14:g.990
    17561_99021465del
    GRCh38 (hg38)NC_000007.14Chr799,017,56199,021,465
    nssv18161313RemappedPerfectNC_000007.13:g.986
    15184_98619088del
    GRCh37.p13First PassNC_000007.13Chr798,615,18498,619,088

    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)
    nssv18161313<0.001139072
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