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nsv6501768

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:981

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 92 SVs from 16 studies. See in: genome view    
    Submitted genomic28,649,636-28,650,616Question Mark
    Overlapping variant regions from other studies: 92 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):26,976,654-26,977,634Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6501768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,649,63628,650,616
    nsv6501768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1726,976,65426,977,634

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18035194deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18035194Submitted genomicNC_000017.11:g.286
    49636_28650616del
    GRCh38 (hg38)NC_000017.11Chr1728,649,63628,650,616
    nssv18035194RemappedPerfectNC_000017.10:g.269
    76654_26977634del
    GRCh37.p13First PassNC_000017.10Chr1726,976,65426,977,634

    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)
    nssv18035194<0.001136346
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