nsv7065616

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:975,158

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2748 SVs from 101 studies. See in: genome view    
    Submitted genomic55,877,934-56,853,091Question Mark
    Overlapping variant regions from other studies: 2751 SVs from 101 studies. See in: genome view    
    Remapped(Score: Perfect):55,645,410-56,620,567Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7065616Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1155,877,93456,853,091
    nsv7065616RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1155,645,41056,620,567

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18742707inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18742707Submitted genomicNC_000011.10:g.558
    77934_56853091inv
    GRCh38 (hg38)NC_000011.10Chr1155,877,93456,853,091
    nssv18742707RemappedPerfectNC_000011.9:g.5564
    5410_56620567inv
    GRCh37.p13First PassNC_000011.9Chr1155,645,41056,620,567

    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)
    nssv187427074e-061276268
    Support Center