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nsv6321189

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:207,662

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 700 SVs from 76 studies. See in: genome view    
    Submitted genomic228,336,437-228,544,098Question Mark
    Overlapping variant regions from other studies: 702 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):228,524,138-228,731,799Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6321189Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1228,336,437228,544,098
    nsv6321189RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1228,524,138228,731,799

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18202728duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18202728Submitted genomicNC_000001.11:g.228
    336437_228544098du
    p
    GRCh38 (hg38)NC_000001.11Chr1228,336,437228,544,098
    nssv18202728RemappedPerfectNC_000001.10:g.228
    524138_228731799du
    p
    GRCh37.p13First PassNC_000001.10Chr1228,524,138228,731,799

    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)
    nssv18202728<0.001139278
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