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nsv6451688

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,130

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 343 SVs from 51 studies. See in: genome view    
    Submitted genomic87,019,399-87,067,528Question Mark
    Overlapping variant regions from other studies: 343 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):88,779,156-88,827,285Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6451688Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1087,019,39987,067,528
    nsv6451688RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1088,779,15688,827,285

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18195155duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18195155Submitted genomicNC_000010.11:g.870
    19399_87067528dup
    GRCh38 (hg38)NC_000010.11Chr1087,019,39987,067,528
    nssv18195155RemappedPerfectNC_000010.10:g.887
    79156_88827285dup
    GRCh37.p13First PassNC_000010.10Chr1088,779,15688,827,285

    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)
    nssv18195155<0.001139258
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