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nsv6875209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 278 SVs from 41 studies. See in: genome view    
    Submitted genomic15,152,901-15,163,500Question Mark
    Overlapping variant regions from other studies: 284 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):15,152,899-15,163,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr915,152,90115,163,500
    nsv6875209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr915,152,89915,163,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18566496deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18566496Submitted genomicNC_000009.12:g.151
    52901_15163500del
    GRCh38 (hg38)NC_000009.12Chr915,152,90115,163,500
    nssv18566496RemappedPerfectNC_000009.11:g.151
    52899_15163498del
    GRCh37.p13First PassNC_000009.11Chr915,152,89915,163,498

    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)
    nssv185664962.9e-058274028
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