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nsv7058619

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,770,671

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4474 SVs from 92 studies. See in: genome view    
    Submitted genomic49,389,100-51,159,770Question Mark
    Overlapping variant regions from other studies: 4475 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):47,466,462-49,237,131Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058619Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1749,389,10051,159,770
    nsv7058619RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1747,466,46249,237,131

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18758972inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18758972Submitted genomicNC_000017.11:g.493
    89100_51159770inv
    GRCh38 (hg38)NC_000017.11Chr1749,389,10051,159,770
    nssv18758972RemappedPerfectNC_000017.10:g.474
    66462_49237131inv
    GRCh37.p13First PassNC_000017.10Chr1747,466,46249,237,131

    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)
    nssv187589724e-061276268
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