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nsv6793310

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,243

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 331 SVs from 51 studies. See in: genome view    
    Submitted genomic20,247,398-20,322,640Question Mark
    Overlapping variant regions from other studies: 331 SVs from 51 studies. See in: genome view    
    Remapped(Score: Perfect):20,247,629-20,322,871Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6793310Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr620,247,39820,322,640
    nsv6793310RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr620,247,62920,322,871

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18523761deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18523761Submitted genomicNC_000006.12:g.202
    47398_20322640del
    GRCh38 (hg38)NC_000006.12Chr620,247,39820,322,640
    nssv18523761RemappedPerfectNC_000006.11:g.202
    47629_20322871del
    GRCh37.p13First PassNC_000006.11Chr620,247,62920,322,871

    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)
    nssv185237614e-061276174
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