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nsv6961566

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 73 SVs from 16 studies. See in: genome view    
    Submitted genomic96,334,678-96,336,977Question Mark
    Overlapping variant regions from other studies: 73 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):96,801,015-96,803,314Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6961566Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1496,334,67896,336,977
    nsv6961566RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1496,801,01596,803,314

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391733deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391733Submitted genomicNC_000014.9:g.9633
    4678_96336977del
    GRCh38 (hg38)NC_000014.9Chr1496,334,67896,336,977
    nssv18391733RemappedPerfectNC_000014.8:g.9680
    1015_96803314del
    GRCh37.p13First PassNC_000014.8Chr1496,801,01596,803,314

    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)
    nssv183917334e-061275678
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