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nsv6994608

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,766,918

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 23805 SVs from 129 studies. See in: genome view    
    Submitted genomic76,392,054-84,158,971Question Mark
    Overlapping variant regions from other studies: 23801 SVs from 129 studies. See in: genome view    
    Remapped(Score: Good):76,425,951-84,192,576Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6994608Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1676,392,05484,158,971
    nsv6994608RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1676,425,95184,192,576

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18624591duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18624591Submitted genomicNC_000016.10:g.763
    92054_84158971dup
    GRCh38 (hg38)NC_000016.10Chr1676,392,05484,158,971
    nssv18624591RemappedGoodNC_000016.9:g.7642
    5951_84192576dup
    GRCh37.p13First PassNC_000016.9Chr1676,425,95184,192,576

    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)
    nssv186245914e-061274850
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