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nsv6905649

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:629

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 27 studies. See in: genome view    
    Submitted genomic4,998,884-4,999,512Question Mark
    Overlapping variant regions from other studies: 100 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):5,020,114-5,020,742Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6905649Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,998,8844,999,512
    nsv6905649RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr115,020,1145,020,742

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351003deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351003Submitted genomicNC_000011.10:g.499
    8884_4999512del
    GRCh38 (hg38)NC_000011.10Chr114,998,8844,999,512
    nssv18351003RemappedPerfectNC_000011.9:g.5020
    114_5020742del
    GRCh37.p13First PassNC_000011.9Chr115,020,1145,020,742

    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)
    nssv183510033.6e-050268560
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