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nsv7047433

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,891

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 149 SVs from 30 studies. See in: genome view    
    Submitted genomic101,971,211-101,974,101Question Mark
    Overlapping variant regions from other studies: 149 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):102,436,767-102,439,657Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047433Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1101,971,211101,974,101
    nsv7047433RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1102,436,767102,439,657

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750778inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750778Submitted genomicNC_000001.11:g.101
    971211_101974101in
    v
    GRCh38 (hg38)NC_000001.11Chr1101,971,211101,974,101
    nssv18750778RemappedPerfectNC_000001.10:g.102
    436767_102439657in
    v
    GRCh37.p13First PassNC_000001.10Chr1102,436,767102,439,657

    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)
    nssv187507783.2e-059274832
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