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nsv6643274

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,310

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 172 SVs from 37 studies. See in: genome view    
    Submitted genomic160,990,054-160,996,363Question Mark
    Overlapping variant regions from other studies: 176 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):160,959,844-160,966,153Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643274Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,990,054160,996,363
    nsv6643274RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,959,844160,966,153

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18363461deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18363461Submitted genomicNC_000001.11:g.160
    990054_160996363de
    l
    GRCh38 (hg38)NC_000001.11Chr1160,990,054160,996,363
    nssv18363461RemappedPerfectNC_000001.10:g.160
    959844_160966153de
    l
    GRCh37.p13First PassNC_000001.10Chr1160,959,844160,966,153

    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)
    nssv183634612.1e-056275450
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