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nsv6977383

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 295 SVs from 39 studies. See in: genome view    
    Submitted genomic28,787,201-28,787,500Question Mark
    Overlapping variant regions from other studies: 297 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):29,032,347-29,032,646Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6977383Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1528,787,20128,787,500
    nsv6977383RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1529,032,34729,032,646

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18392471deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18392471Submitted genomicNC_000015.10:g.287
    87201_28787500del
    GRCh38 (hg38)NC_000015.10Chr1528,787,20128,787,500
    nssv18392471RemappedPerfectNC_000015.9:g.2903
    2347_29032646del
    GRCh37.p13First PassNC_000015.9Chr1529,032,34729,032,646

    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)
    nssv183924710.09522216241274
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