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nsv6552704

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,482

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Submitted genomic50,131,972-50,136,453Question Mark
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):48,748,509-48,752,990Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6552704Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2050,131,97250,136,453
    nsv6552704RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2048,748,50948,752,990

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18069048deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18069048Submitted genomicNC_000020.11:g.501
    31972_50136453del
    GRCh38 (hg38)NC_000020.11Chr2050,131,97250,136,453
    nssv18069048RemappedPerfectNC_000020.10:g.487
    48509_48752990del
    GRCh37.p13First PassNC_000020.10Chr2048,748,50948,752,990

    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)
    nssv18069048<0.001139068
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