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nsv7045478

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,429,809

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 10731 SVs from 119 studies. See in: genome view    
    Submitted genomic184,811,410-187,241,218Question Mark
    Overlapping variant regions from other studies: 10731 SVs from 119 studies. See in: genome view    
    Remapped(Score: Perfect):185,732,564-188,162,372Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045478Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4184,811,410187,241,218
    nsv7045478RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4185,732,564188,162,372

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774006inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774006Submitted genomicNC_000004.12:g.184
    811410_187241218in
    v
    GRCh38 (hg38)NC_000004.12Chr4184,811,410187,241,218
    nssv18774006RemappedPerfectNC_000004.11:g.185
    732564_188162372in
    v
    GRCh37.p13First PassNC_000004.11Chr4185,732,564188,162,372

    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)
    nssv18774006<0.00153274644
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