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nsv6658068

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,992

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 154 SVs from 28 studies. See in: genome view    
    Submitted genomic99,902,295-99,907,286Question Mark
    Overlapping variant regions from other studies: 154 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):100,367,851-100,372,842Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6658068Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr199,902,29599,907,286
    nsv6658068RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1100,367,851100,372,842

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18429209deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18429209Submitted genomicNC_000001.11:g.999
    02295_99907286del
    GRCh38 (hg38)NC_000001.11Chr199,902,29599,907,286
    nssv18429209RemappedPerfectNC_000001.10:g.100
    367851_100372842de
    l
    GRCh37.p13First PassNC_000001.10Chr1100,367,851100,372,842

    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)
    nssv184292094e-061276252
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