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nsv6992817

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:356

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Submitted genomic65,443,882-65,444,237Question Mark
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):65,477,785-65,478,140Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992817Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1665,443,88265,444,237
    nsv6992817RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1665,477,78565,478,140

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18622972duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18622972Submitted genomicNC_000016.10:g.654
    43882_65444237dup
    GRCh38 (hg38)NC_000016.10Chr1665,443,88265,444,237
    nssv18622972RemappedPerfectNC_000016.9:g.6547
    7785_65478140dup
    GRCh37.p13First PassNC_000016.9Chr1665,477,78565,478,140

    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)
    nssv186229724e-061241386
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