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nsv6918892

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,287

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 152 SVs from 28 studies. See in: genome view    
    Submitted genomic4,833,776-4,836,062Question Mark
    Overlapping variant regions from other studies: 152 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):4,942,942-4,945,228Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6918892Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr124,833,7764,836,062
    nsv6918892RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr124,942,9424,945,228

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18361110deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18361110Submitted genomicNC_000012.12:g.483
    3776_4836062del
    GRCh38 (hg38)NC_000012.12Chr124,833,7764,836,062
    nssv18361110RemappedPerfectNC_000012.11:g.494
    2942_4945228del
    GRCh37.p13First PassNC_000012.11Chr124,942,9424,945,228

    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)
    nssv183611104e-061274942
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