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nsv7052639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,838

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 222 SVs from 39 studies. See in: genome view    
    Submitted genomic101,950,587-101,976,424Question Mark
    Overlapping variant regions from other studies: 222 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):102,416,143-102,441,980Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1101,950,587101,976,424
    nsv7052639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1102,416,143102,441,980

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747394inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747394Submitted genomicNC_000001.11:g.101
    950587_101976424in
    v
    GRCh38 (hg38)NC_000001.11Chr1101,950,587101,976,424
    nssv18747394RemappedPerfectNC_000001.10:g.102
    416143_102441980in
    v
    GRCh37.p13First PassNC_000001.10Chr1102,416,143102,441,980

    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)
    nssv187473944e-061276268
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