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nsv7048086

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,505,891

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 17722 SVs from 122 studies. See in: genome view    
    Submitted genomic100,058,481-107,564,371Question Mark
    Overlapping variant regions from other studies: 17743 SVs from 122 studies. See in: genome view    
    Remapped(Score: Perfect):100,979,638-108,485,528Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048086Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4100,058,481107,564,371
    nsv7048086RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4100,979,638108,485,528

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771832inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771832Submitted genomicNC_000004.12:g.100
    058481_107564371in
    v
    GRCh38 (hg38)NC_000004.12Chr4100,058,481107,564,371
    nssv18771832RemappedPerfectNC_000004.11:g.100
    979638_108485528in
    v
    GRCh37.p13First PassNC_000004.11Chr4100,979,638108,485,528

    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)
    nssv187718324e-061276268
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