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nsv7011165

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,994

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 25 studies. See in: genome view    
    Submitted genomic18,378,584-18,383,577Question Mark
    Overlapping variant regions from other studies: 104 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):18,489,394-18,494,387Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7011165Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1918,378,58418,383,577
    nsv7011165RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1918,489,39418,494,387

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18639392duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18639392Submitted genomicNC_000019.10:g.183
    78584_18383577dup
    GRCh38 (hg38)NC_000019.10Chr1918,378,58418,383,577
    nssv18639392RemappedPerfectNC_000019.9:g.1848
    9394_18494387dup
    GRCh37.p13First PassNC_000019.9Chr1918,489,39418,494,387

    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)
    nssv186393923.6e-0510275254
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