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nsv6780678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,108

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 77 SVs from 13 studies. See in: genome view    
    Submitted genomic149,038,953-149,041,060Question Mark
    Overlapping variant regions from other studies: 77 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):148,418,516-148,420,623Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6780678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5149,038,953149,041,060
    nsv6780678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5148,418,516148,420,623

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18507230deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18507230Submitted genomicNC_000005.10:g.149
    038953_149041060de
    l
    GRCh38 (hg38)NC_000005.10Chr5149,038,953149,041,060
    nssv18507230RemappedPerfectNC_000005.9:g.1484
    18516_148420623del
    GRCh37.p13First PassNC_000005.9Chr5148,418,516148,420,623

    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)
    nssv185072301.1e-053274308
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