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nsv6967231

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,923

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 124 SVs from 21 studies. See in: genome view    
    Submitted genomic43,282,345-43,292,267Question Mark
    Overlapping variant regions from other studies: 124 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):43,574,543-43,584,465Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6967231Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1543,282,34543,292,267
    nsv6967231RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1543,574,54343,584,465

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18393838deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18393838Submitted genomicNC_000015.10:g.432
    82345_43292267del
    GRCh38 (hg38)NC_000015.10Chr1543,282,34543,292,267
    nssv18393838RemappedPerfectNC_000015.9:g.4357
    4543_43584465del
    GRCh37.p13First PassNC_000015.9Chr1543,574,54343,584,465

    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)
    nssv18393838<0.00140276016
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