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nsv6644569

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:282,278

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 750 SVs from 68 studies. See in: genome view    
    Submitted genomic171,089,340-171,371,617Question Mark
    Overlapping variant regions from other studies: 753 SVs from 68 studies. See in: genome view    
    Remapped(Score: Good):171,058,481-171,340,756Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644569Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1171,089,340171,371,617
    nsv6644569RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1171,058,481171,340,756

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18362928deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18362928Submitted genomicNC_000001.11:g.171
    089340_171371617de
    l
    GRCh38 (hg38)NC_000001.11Chr1171,089,340171,371,617
    nssv18362928RemappedGoodNC_000001.10:g.171
    058481_171340756de
    l
    GRCh37.p13First PassNC_000001.10Chr1171,058,481171,340,756

    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)
    nssv183629284e-061276022
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