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nsv6332578

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:773

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 16 studies. See in: genome view    
    Submitted genomic94,316,529-94,317,301Question Mark
    Overlapping variant regions from other studies: 114 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):94,782,085-94,782,857Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6332578Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr194,316,52994,317,301
    nsv6332578RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr194,782,08594,782,857

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18065625deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18065625Submitted genomicNC_000001.11:g.943
    16529_94317301del
    GRCh38 (hg38)NC_000001.11Chr194,316,52994,317,301
    nssv18065625RemappedPerfectNC_000001.10:g.947
    82085_94782857del
    GRCh37.p13First PassNC_000001.10Chr194,782,08594,782,857

    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)
    nssv18065625<0.001738428
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