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nsv6789812

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 243 SVs from 44 studies. See in: genome view    
    Submitted genomic44,178,301-44,185,000Question Mark
    Overlapping variant regions from other studies: 243 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):44,146,038-44,152,737Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6789812Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr644,178,30144,185,000
    nsv6789812RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr644,146,03844,152,737

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18525991deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18525991Submitted genomicNC_000006.12:g.441
    78301_44185000del
    GRCh38 (hg38)NC_000006.12Chr644,178,30144,185,000
    nssv18525991RemappedPerfectNC_000006.11:g.441
    46038_44152737del
    GRCh37.p13First PassNC_000006.11Chr644,146,03844,152,737

    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)
    nssv185259912.1e-056275968
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