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nsv6990849

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:247,241

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 937 SVs from 62 studies. See in: genome view    
    Submitted genomic1,282,730-1,529,970Question Mark
    Overlapping variant regions from other studies: 937 SVs from 62 studies. See in: genome view    
    Remapped(Score: Perfect):1,282,731-1,529,971Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990849Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr181,282,7301,529,970
    nsv6990849RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr181,282,7311,529,971

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18632911duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18632911Submitted genomicNC_000018.10:g.128
    2730_1529970dup
    GRCh38 (hg38)NC_000018.10Chr181,282,7301,529,970
    nssv18632911RemappedPerfectNC_000018.9:g.1282
    731_1529971dup
    GRCh37.p13First PassNC_000018.9Chr181,282,7311,529,971

    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)
    nssv186329114e-061273686
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