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nsv6655662

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,201

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 208 SVs from 42 studies. See in: genome view    
    Submitted genomic86,615,917-86,636,117Question Mark
    Overlapping variant regions from other studies: 208 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):87,081,600-87,101,800Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6655662Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr186,615,91786,636,117
    nsv6655662RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr187,081,60087,101,800

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18427661deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18427661Submitted genomicNC_000001.11:g.866
    15917_86636117del
    GRCh38 (hg38)NC_000001.11Chr186,615,91786,636,117
    nssv18427661RemappedPerfectNC_000001.10:g.870
    81600_87101800del
    GRCh37.p13First PassNC_000001.10Chr187,081,60087,101,800

    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)
    nssv184276617e-062275488
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