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nsv7077519

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,637,582

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 12131 SVs from 118 studies. See in: genome view    
    Submitted genomic86,495,718-92,133,299Question Mark
    Overlapping variant regions from other studies: 12131 SVs from 118 studies. See in: genome view    
    Remapped(Score: Perfect):86,889,495-92,527,075Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077519Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1286,495,71892,133,299
    nsv7077519RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1286,889,49592,527,075

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753214inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753214Submitted genomicNC_000012.12:g.864
    95718_92133299inv
    GRCh38 (hg38)NC_000012.12Chr1286,495,71892,133,299
    nssv18753214RemappedPerfectNC_000012.11:g.868
    89495_92527075inv
    GRCh37.p13First PassNC_000012.11Chr1286,889,49592,527,075

    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)
    nssv187532144e-061276268
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