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nsv6968122

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,506

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 554 SVs from 50 studies. See in: genome view    
    Submitted genomic25,247,681-25,251,186Question Mark
    Overlapping variant regions from other studies: 554 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):25,492,828-25,496,333Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6968122Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1525,247,68125,251,186
    nsv6968122RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1525,492,82825,496,333

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18393191deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18393191Submitted genomicNC_000015.10:g.252
    47681_25251186del
    GRCh38 (hg38)NC_000015.10Chr1525,247,68125,251,186
    nssv18393191RemappedPerfectNC_000015.9:g.2549
    2828_25496333del
    GRCh37.p13First PassNC_000015.9Chr1525,492,82825,496,333

    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)
    nssv183931911.8e-055275774
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