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nsv7060892

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,137

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 19 studies. See in: genome view    
    Submitted genomic127,314,416-127,316,552Question Mark
    Overlapping variant regions from other studies: 104 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):130,076,695-130,078,831Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7060892Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9127,314,416127,316,552
    nsv7060892RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9130,076,695130,078,831

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784742inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784742Submitted genomicNC_000009.12:g.127
    314416_127316552in
    v
    GRCh38 (hg38)NC_000009.12Chr9127,314,416127,316,552
    nssv18784742RemappedPerfectNC_000009.11:g.130
    076695_130078831in
    v
    GRCh37.p13First PassNC_000009.11Chr9130,076,695130,078,831

    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)
    nssv187847421.1e-053274672
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