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nsv6439355

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:624

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 75 SVs from 17 studies. See in: genome view    
    Submitted genomic18,661,437-18,662,060Question Mark
    Overlapping variant regions from other studies: 75 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):18,950,366-18,950,989Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6439355Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1018,661,43718,662,060
    nsv6439355RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1018,950,36618,950,989

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17980811deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17980811Submitted genomicNC_000010.11:g.186
    61437_18662060del
    GRCh38 (hg38)NC_000010.11Chr1018,661,43718,662,060
    nssv17980811RemappedPerfectNC_000010.10:g.189
    50366_18950989del
    GRCh37.p13First PassNC_000010.10Chr1018,950,36618,950,989

    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)
    nssv17980811<0.001135158
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