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nsv6800320

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41,264

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 298 SVs from 49 studies. See in: genome view    
    Submitted genomic2,398,427-2,439,690Question Mark
    Overlapping variant regions from other studies: 298 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):2,438,062-2,479,325Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6800320Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr72,398,4272,439,690
    nsv6800320RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr72,438,0622,479,325

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18540110deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18540110Submitted genomicNC_000007.14:g.239
    8427_2439690del
    GRCh38 (hg38)NC_000007.14Chr72,398,4272,439,690
    nssv18540110RemappedPerfectNC_000007.13:g.243
    8062_2479325del
    GRCh37.p13First PassNC_000007.13Chr72,438,0622,479,325

    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)
    nssv185401104e-061276242
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