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nsv6334195

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 24 studies. See in: genome view    
    Submitted genomic171,527,231-171,528,330Question Mark
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):171,496,370-171,497,469Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6334195Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1171,527,231171,528,330
    nsv6334195RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1171,496,370171,497,469

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053828deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053828Submitted genomicNC_000001.11:g.171
    527231_171528330de
    l
    GRCh38 (hg38)NC_000001.11Chr1171,527,231171,528,330
    nssv18053828RemappedPerfectNC_000001.10:g.171
    496370_171497469de
    l
    GRCh37.p13First PassNC_000001.10Chr1171,496,370171,497,469

    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)
    nssv18053828<0.001138018
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