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nsv7046675

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,139,696

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3101 SVs from 98 studies. See in: genome view    
    Submitted genomic101,693,247-102,832,942Question Mark
    Overlapping variant regions from other studies: 3101 SVs from 98 studies. See in: genome view    
    Remapped(Score: Perfect):102,158,803-103,298,498Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046675Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1101,693,247102,832,942
    nsv7046675RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1102,158,803103,298,498

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18731514inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18731514Submitted genomicNC_000001.11:g.101
    693247_102832942in
    v
    GRCh38 (hg38)NC_000001.11Chr1101,693,247102,832,942
    nssv18731514RemappedPerfectNC_000001.10:g.102
    158803_103298498in
    v
    GRCh37.p13First PassNC_000001.10Chr1102,158,803103,298,498

    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)
    nssv187315147e-062274590
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