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nsv7048581

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:456,505

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1113 SVs from 71 studies. See in: genome view    
    Submitted genomic174,019,781-174,476,285Question Mark
    Overlapping variant regions from other studies: 1116 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):173,988,919-174,445,423Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048581Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1174,019,781174,476,285
    nsv7048581RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,988,919174,445,423

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18747466inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18747466Submitted genomicNC_000001.11:g.174
    019781_174476285in
    v
    GRCh38 (hg38)NC_000001.11Chr1174,019,781174,476,285
    nssv18747466RemappedPerfectNC_000001.10:g.173
    988919_174445423in
    v
    GRCh37.p13First PassNC_000001.10Chr1173,988,919174,445,423

    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)
    nssv187474667e-062274642
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