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nsv7048464

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,945

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 192 SVs from 33 studies. See in: genome view    
    Submitted genomic150,455,239-150,468,183Question Mark
    Overlapping variant regions from other studies: 192 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):150,152,327-150,165,271Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048464Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7150,455,239150,468,183
    nsv7048464RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7150,152,327150,165,271

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18782094inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18782094Submitted genomicNC_000007.14:g.150
    455239_150468183in
    v
    GRCh38 (hg38)NC_000007.14Chr7150,455,239150,468,183
    nssv18782094RemappedPerfectNC_000007.13:g.150
    152327_150165271in
    v
    GRCh37.p13First PassNC_000007.13Chr7150,152,327150,165,271

    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)
    nssv187820944e-061276268
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