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nsv6330458

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:202,842

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1194 SVs from 86 studies. See in: genome view    
    Submitted genomic108,984,462-109,187,303Question Mark
    Overlapping variant regions from other studies: 1195 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):109,527,084-109,729,925Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6330458Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1108,984,462109,187,303
    nsv6330458RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1109,527,084109,729,925

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18199235duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18199235Submitted genomicNC_000001.11:g.108
    984462_109187303du
    p
    GRCh38 (hg38)NC_000001.11Chr1108,984,462109,187,303
    nssv18199235RemappedPerfectNC_000001.10:g.109
    527084_109729925du
    p
    GRCh37.p13First PassNC_000001.10Chr1109,527,084109,729,925

    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)
    nssv18199235<0.001139270
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