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nsv6747927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 37 studies. See in: genome view    
    Submitted genomic151,099,451-151,099,476Question Mark
    Overlapping variant regions from other studies: 193 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):152,020,603-152,020,628Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6747927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4151,099,451151,099,476
    nsv6747927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4152,020,603152,020,628

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18492100deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18492100Submitted genomicNC_000004.12:g.151
    099451_151099476de
    l
    GRCh38 (hg38)NC_000004.12Chr4151,099,451151,099,476
    nssv18492100RemappedPerfectNC_000004.11:g.152
    020603_152020628de
    l
    GRCh37.p13First PassNC_000004.11Chr4152,020,603152,020,628

    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)
    nssv18492100<0.001135253682
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