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nsv6320390

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:363

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 19 studies. See in: genome view    
    Submitted genomic159,186,250-159,186,612Question Mark
    Overlapping variant regions from other studies: 109 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):159,156,040-159,156,402Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6320390Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1159,186,250159,186,612
    nsv6320390RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1159,156,040159,156,402

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053502deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053502Submitted genomicNC_000001.11:g.159
    186250_159186612de
    l
    GRCh38 (hg38)NC_000001.11Chr1159,186,250159,186,612
    nssv18053502RemappedPerfectNC_000001.10:g.159
    156040_159156402de
    l
    GRCh37.p13First PassNC_000001.10Chr1159,156,040159,156,402

    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)
    nssv18053502<0.001134688
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