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nsv6861524

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 25 studies. See in: genome view    
    Submitted genomic87,859,247-87,859,310Question Mark
    Overlapping variant regions from other studies: 107 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):90,474,162-90,474,225Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6861524Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr987,859,24787,859,310
    nsv6861524RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr990,474,16290,474,225

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18585224deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18585224Submitted genomicNC_000009.12:g.878
    59247_87859310del
    GRCh38 (hg38)NC_000009.12Chr987,859,24787,859,310
    nssv18585224RemappedPerfectNC_000009.11:g.904
    74162_90474225del
    GRCh37.p13First PassNC_000009.11Chr990,474,16290,474,225

    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)
    nssv185852240.004964253292
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