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nsv6650551

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:141,435

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 375 SVs from 40 studies. See in: genome view    
    Submitted genomic46,413,879-46,555,313Question Mark
    Overlapping variant regions from other studies: 375 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):46,879,551-47,020,985Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6650551Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr146,413,87946,555,313
    nsv6650551RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr146,879,55147,020,985

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18390777deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18390777Submitted genomicNC_000001.11:g.464
    13879_46555313del
    GRCh38 (hg38)NC_000001.11Chr146,413,87946,555,313
    nssv18390777RemappedPerfectNC_000001.10:g.468
    79551_47020985del
    GRCh37.p13First PassNC_000001.10Chr146,879,55147,020,985

    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)
    nssv183907774e-061276262
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