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nsv6454666

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 76 SVs from 17 studies. See in: genome view    
    Submitted genomic91,487,101-91,487,900Question Mark
    Overlapping variant regions from other studies: 76 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):93,246,858-93,247,657Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6454666Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1091,487,10191,487,900
    nsv6454666RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1093,246,85893,247,657

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17985358deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17985358Submitted genomicNC_000010.11:g.914
    87101_91487900del
    GRCh38 (hg38)NC_000010.11Chr1091,487,10191,487,900
    nssv17985358RemappedPerfectNC_000010.10:g.932
    46858_93247657del
    GRCh37.p13First PassNC_000010.10Chr1093,246,85893,247,657

    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)
    nssv17985358<0.001637988
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