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nsv6990526

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Submitted genomic28,743,522-28,743,571Question Mark
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):27,070,540-27,070,589Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6990526Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,743,52228,743,571
    nsv6990526RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1727,070,54027,070,589

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18406285deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18406285Submitted genomicNC_000017.11:g.287
    43522_28743571del
    GRCh38 (hg38)NC_000017.11Chr1728,743,52228,743,571
    nssv18406285RemappedPerfectNC_000017.10:g.270
    70540_27070589del
    GRCh37.p13First PassNC_000017.10Chr1727,070,54027,070,589

    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)
    nssv184062854e-061248316
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