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nsv6545693

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:293

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 20 studies. See in: genome view    
    Submitted genomic44,393,639-44,393,931Question Mark
    Overlapping variant regions from other studies: 132 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):43,022,279-43,022,571Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6545693Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2044,393,63944,393,931
    nsv6545693RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,022,27943,022,571

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18067824deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18067824Submitted genomicNC_000020.11:g.443
    93639_44393931del
    GRCh38 (hg38)NC_000020.11Chr2044,393,63944,393,931
    nssv18067824RemappedPerfectNC_000020.10:g.430
    22279_43022571del
    GRCh37.p13First PassNC_000020.10Chr2043,022,27943,022,571

    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)
    nssv18067824<0.001432178
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