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nsv6883106

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,990

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 21 studies. See in: genome view    
    Submitted genomic69,243,241-69,247,230Question Mark
    Overlapping variant regions from other studies: 90 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):71,002,997-71,006,986Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6883106Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1069,243,24169,247,230
    nsv6883106RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1071,002,99771,006,986

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18339083deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18339083Submitted genomicNC_000010.11:g.692
    43241_69247230del
    GRCh38 (hg38)NC_000010.11Chr1069,243,24169,247,230
    nssv18339083RemappedPerfectNC_000010.10:g.710
    02997_71006986del
    GRCh37.p13First PassNC_000010.10Chr1071,002,99771,006,986

    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)
    nssv183390834e-061276178
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