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nsv6902229

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 250 SVs from 46 studies. See in: genome view    
    Submitted genomic106,182,301-106,262,400Question Mark
    Overlapping variant regions from other studies: 250 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):106,053,028-106,133,127Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6902229Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11106,182,301106,262,400
    nsv6902229RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11106,053,028106,133,127

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18342388deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18342388Submitted genomicNC_000011.10:g.106
    182301_106262400de
    l
    GRCh38 (hg38)NC_000011.10Chr11106,182,301106,262,400
    nssv18342388RemappedPerfectNC_000011.9:g.1060
    53028_106133127del
    GRCh37.p13First PassNC_000011.9Chr11106,053,028106,133,127

    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)
    nssv183423884e-061275690
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