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nsv6330654

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,153

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 28 studies. See in: genome view    
    Submitted genomic177,364,103-177,380,255Question Mark
    Overlapping variant regions from other studies: 167 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):177,333,239-177,349,391Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6330654Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1177,364,103177,380,255
    nsv6330654RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1177,333,239177,349,391

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18053791deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18053791Submitted genomicNC_000001.11:g.177
    364103_177380255de
    l
    GRCh38 (hg38)NC_000001.11Chr1177,364,103177,380,255
    nssv18053791RemappedPerfectNC_000001.10:g.177
    333239_177349391de
    l
    GRCh37.p13First PassNC_000001.10Chr1177,333,239177,349,391

    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)
    nssv18053791<0.001139128
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