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nsv6321454

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:359,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1756 SVs from 91 studies. See in: genome view    
    Submitted genomic189,270,601-189,630,300Question Mark
    Overlapping variant regions from other studies: 1756 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):189,239,732-189,599,430Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6321454Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1189,270,601189,630,300
    nsv6321454RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1189,239,732189,599,430

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18054996deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18054996Submitted genomicNC_000001.11:g.189
    270601_189630300de
    l
    GRCh38 (hg38)NC_000001.11Chr1189,270,601189,630,300
    nssv18054996RemappedPerfectNC_000001.10:g.189
    239732_189599430de
    l
    GRCh37.p13First PassNC_000001.10Chr1189,239,732189,599,430

    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)
    nssv18054996<0.001338930
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