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nsv6441598

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:335

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 71 SVs from 15 studies. See in: genome view    
    Submitted genomic33,758,024-33,758,358Question Mark
    Overlapping variant regions from other studies: 71 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):34,046,952-34,047,286Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6441598Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1033,758,02433,758,358
    nsv6441598RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1034,046,95234,047,286

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17979784deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17979784Submitted genomicNC_000010.11:g.337
    58024_33758358del
    GRCh38 (hg38)NC_000010.11Chr1033,758,02433,758,358
    nssv17979784RemappedPerfectNC_000010.10:g.340
    46952_34047286del
    GRCh37.p13First PassNC_000010.10Chr1034,046,95234,047,286

    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)
    nssv17979784<0.001233018
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