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nsv7043937

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Submitted genomic144,020,774-144,020,793Question Mark
    Overlapping variant regions from other studies: 82 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):144,341,911-144,341,930Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043937Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6144,020,774144,020,793
    nsv7043937RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6144,341,911144,341,930

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778406inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778406Submitted genomicNC_000006.12:g.144
    020774_144020793in
    v
    GRCh38 (hg38)NC_000006.12Chr6144,020,774144,020,793
    nssv18778406RemappedPerfectNC_000006.11:g.144
    341911_144341930in
    v
    GRCh37.p13First PassNC_000006.11Chr6144,341,911144,341,930

    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)
    nssv187784064e-061276250
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