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nsv7044121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,270

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 162 SVs from 33 studies. See in: genome view    
    Submitted genomic158,448,295-158,473,564Question Mark
    Overlapping variant regions from other studies: 166 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):158,418,085-158,443,354Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1158,448,295158,473,564
    nsv7044121RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1158,418,085158,443,354

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743516inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743516Submitted genomicNC_000001.11:g.158
    448295_158473564in
    v
    GRCh38 (hg38)NC_000001.11Chr1158,448,295158,473,564
    nssv18743516RemappedPerfectNC_000001.10:g.158
    418085_158443354in
    v
    GRCh37.p13First PassNC_000001.10Chr1158,418,085158,443,354

    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)
    nssv187435164e-061276268
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