nsv6672996

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,583

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 197 SVs from 29 studies. See in: genome view    
    Submitted genomic241,557,019-241,563,601Question Mark
    Overlapping variant regions from other studies: 200 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):241,720,319-241,726,901Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6672996Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1241,557,019241,563,601
    nsv6672996RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1241,720,319241,726,901

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18368904deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18368904Submitted genomicNC_000001.11:g.241
    557019_241563601de
    l
    GRCh38 (hg38)NC_000001.11Chr1241,557,019241,563,601
    nssv18368904RemappedPerfectNC_000001.10:g.241
    720319_241726901de
    l
    GRCh37.p13First PassNC_000001.10Chr1241,720,319241,726,901

    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)
    nssv183689044e-061276234
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