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nsv6655927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:374

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 17 studies. See in: genome view    
    Submitted genomic84,810,436-84,810,809Question Mark
    Overlapping variant regions from other studies: 120 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):85,276,119-85,276,492Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6655927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr184,810,43684,810,809
    nsv6655927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr185,276,11985,276,492

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640537duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640537Submitted genomicNC_000001.11:g.848
    10436_84810809dup
    GRCh38 (hg38)NC_000001.11Chr184,810,43684,810,809
    nssv18640537RemappedPerfectNC_000001.10:g.852
    76119_85276492dup
    GRCh37.p13First PassNC_000001.10Chr185,276,11985,276,492

    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)
    nssv186405376.2e-0515237452
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