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nsv7039342

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,830,159

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15217 SVs from 121 studies. See in: genome view    
    Submitted genomic86,041,090-92,871,248Question Mark
    Overlapping variant regions from other studies: 15217 SVs from 121 studies. See in: genome view    
    Remapped(Score: Perfect):86,750,808-93,580,966Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039342Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr686,041,09092,871,248
    nsv7039342RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr686,750,80893,580,966

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780565inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780565Submitted genomicNC_000006.12:g.860
    41090_92871248inv
    GRCh38 (hg38)NC_000006.12Chr686,041,09092,871,248
    nssv18780565RemappedPerfectNC_000006.11:g.867
    50808_93580966inv
    GRCh37.p13First PassNC_000006.11Chr686,750,80893,580,966

    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)
    nssv18780565<0.001125271938
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