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nsv6419421

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77,329

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 328 SVs from 49 studies. See in: genome view    
    Submitted genomic57,360,079-57,437,407Question Mark
    Overlapping variant regions from other studies: 328 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):58,272,638-58,349,966Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6419421Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr857,360,07957,437,407
    nsv6419421RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr858,272,63858,349,966

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18169880deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18169880Submitted genomicNC_000008.11:g.573
    60079_57437407del
    GRCh38 (hg38)NC_000008.11Chr857,360,07957,437,407
    nssv18169880RemappedPerfectNC_000008.10:g.582
    72638_58349966del
    GRCh37.p13First PassNC_000008.10Chr858,272,63858,349,966

    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)
    nssv18169880<0.001139276
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