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nsv6902707

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,823

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 25 studies. See in: genome view    
    Submitted genomic67,130,890-67,134,712Question Mark
    Overlapping variant regions from other studies: 84 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):66,898,361-66,902,183Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6902707Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1167,130,89067,134,712
    nsv6902707RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1166,898,36166,902,183

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353085deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353085Submitted genomicNC_000011.10:g.671
    30890_67134712del
    GRCh38 (hg38)NC_000011.10Chr1167,130,89067,134,712
    nssv18353085RemappedPerfectNC_000011.9:g.6689
    8361_66902183del
    GRCh37.p13First PassNC_000011.9Chr1166,898,36166,902,183

    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)
    nssv183530854e-061276228
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