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nsv7034349

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:111

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 27 studies. See in: genome view    
    Submitted genomic50,117,805-50,117,915Question Mark
    Overlapping variant regions from other studies: 104 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):48,734,342-48,734,452Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7034349Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2050,117,80550,117,915
    nsv7034349RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2048,734,34248,734,452

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18432228deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18432228Submitted genomicNC_000020.11:g.501
    17805_50117915del
    GRCh38 (hg38)NC_000020.11Chr2050,117,80550,117,915
    nssv18432228RemappedPerfectNC_000020.10:g.487
    34342_48734452del
    GRCh37.p13First PassNC_000020.10Chr2048,734,34248,734,452

    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)
    nssv184322280.0153894255500
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