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nsv6975749

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 47 studies. See in: genome view    
    Submitted genomic47,414,101-47,433,000Question Mark
    Overlapping variant regions from other studies: 174 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):47,706,298-47,725,197Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6975749Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1547,414,10147,433,000
    nsv6975749RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1547,706,29847,725,197

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18394361deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18394361Submitted genomicNC_000015.10:g.474
    14101_47433000del
    GRCh38 (hg38)NC_000015.10Chr1547,414,10147,433,000
    nssv18394361RemappedPerfectNC_000015.9:g.4770
    6298_47725197del
    GRCh37.p13First PassNC_000015.9Chr1547,706,29847,725,197

    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)
    nssv183943614e-061275620
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