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nsv6328504

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,440

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 21 studies. See in: genome view    
    Submitted genomic11,998,170-11,999,609Question Mark
    Overlapping variant regions from other studies: 138 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):12,058,227-12,059,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6328504Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr111,998,17011,999,609
    nsv6328504RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr112,058,22712,059,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18051293deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18051293Submitted genomicNC_000001.11:g.119
    98170_11999609del
    GRCh38 (hg38)NC_000001.11Chr111,998,17011,999,609
    nssv18051293RemappedPerfectNC_000001.10:g.120
    58227_12059666del
    GRCh37.p13First PassNC_000001.10Chr112,058,22712,059,666

    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)
    nssv18051293<0.001338694
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