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nsv7054819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,790,550

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9585 SVs from 119 studies. See in: genome view    
    Submitted genomic112,393,108-116,183,657Question Mark
    Overlapping variant regions from other studies: 9585 SVs from 119 studies. See in: genome view    
    Remapped(Score: Perfect):111,728,805-115,519,354Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7054819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5112,393,108116,183,657
    nsv7054819RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5111,728,805115,519,354

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18774444inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18774444Submitted genomicNC_000005.10:g.112
    393108_116183657in
    v
    GRCh38 (hg38)NC_000005.10Chr5112,393,108116,183,657
    nssv18774444RemappedPerfectNC_000005.9:g.1117
    28805_115519354inv
    GRCh37.p13First PassNC_000005.9Chr5111,728,805115,519,354

    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)
    nssv187744447e-062276106
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