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nsv6459058

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 248 SVs from 44 studies. See in: genome view    
    Submitted genomic21,656,201-21,681,800Question Mark
    Overlapping variant regions from other studies: 248 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):21,809,135-21,834,734Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6459058Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1221,656,20121,681,800
    nsv6459058RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1221,809,13521,834,734

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18180289duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18180289Submitted genomicNC_000012.12:g.216
    56201_21681800dup
    GRCh38 (hg38)NC_000012.12Chr1221,656,20121,681,800
    nssv18180289RemappedPerfectNC_000012.11:g.218
    09135_21834734dup
    GRCh37.p13First PassNC_000012.11Chr1221,809,13521,834,734

    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)
    nssv18180289<0.0011139214
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