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nsv6329058

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:739

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 23 studies. See in: genome view    
    Submitted genomic98,009,601-98,010,339Question Mark
    Overlapping variant regions from other studies: 119 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):98,475,157-98,475,895Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6329058Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr198,009,60198,010,339
    nsv6329058RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr198,475,15798,475,895

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065783deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065783Submitted genomicNC_000001.11:g.980
    09601_98010339del
    GRCh38 (hg38)NC_000001.11Chr198,009,60198,010,339
    nssv18065783RemappedPerfectNC_000001.10:g.984
    75157_98475895del
    GRCh37.p13First PassNC_000001.10Chr198,475,15798,475,895

    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)
    nssv18065783<0.0011438392
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