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nsv6641887

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,402

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 304 SVs from 51 studies. See in: genome view    
    Submitted genomic148,421,088-148,423,489Question Mark
    Overlapping variant regions from other studies: 51 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):5,236,501-5,238,902Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6641887Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1148,421,088148,423,489
    nsv6641887RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871055.3Chr1|NW_00
    3871055.3
    5,236,5015,238,902

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18350975deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18350975Submitted genomicNC_000001.11:g.148
    421088_148423489de
    l
    GRCh38 (hg38)NC_000001.11Chr1148,421,088148,423,489
    nssv18350975RemappedPerfectNW_003871055.3:g.5
    236501_5238902del
    GRCh37.p13First PassNW_003871055.3Chr1|NW_00
    3871055.3
    5,236,5015,238,902

    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)
    nssv183509752.8e-058276212
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