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nsv6609772

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,763

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 38 studies. See in: genome view    
    Submitted genomic56,030,638-56,032,400Question Mark
    Overlapping variant regions from other studies: 121 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):56,098,331-56,100,093Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6609772Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr756,030,63856,032,400
    nsv6609772RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr756,098,33156,100,093

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18157147deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18157147Submitted genomicNC_000007.14:g.560
    30638_56032400del
    GRCh38 (hg38)NC_000007.14Chr756,030,63856,032,400
    nssv18157147RemappedPerfectNC_000007.13:g.560
    98331_56100093del
    GRCh37.p13First PassNC_000007.13Chr756,098,33156,100,093

    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)
    nssv18157147<0.001338472
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