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nsv6328123

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:595

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 25 studies. See in: genome view    
    Submitted genomic38,919,825-38,920,419Question Mark
    Overlapping variant regions from other studies: 110 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):39,385,497-39,386,091Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6328123Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr138,919,82538,920,419
    nsv6328123RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr139,385,49739,386,091

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18060070deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18060070Submitted genomicNC_000001.11:g.389
    19825_38920419del
    GRCh38 (hg38)NC_000001.11Chr138,919,82538,920,419
    nssv18060070RemappedPerfectNC_000001.10:g.393
    85497_39386091del
    GRCh37.p13First PassNC_000001.10Chr139,385,49739,386,091

    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)
    nssv18060070<0.001535214
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