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nsv7039962

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,362

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 75 SVs from 19 studies. See in: genome view    
    Submitted genomic42,539,280-42,549,641Question Mark
    Overlapping variant regions from other studies: 75 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):42,580,772-42,591,133Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039962Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr342,539,28042,549,641
    nsv7039962RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr342,580,77242,591,133

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18771276inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18771276Submitted genomicNC_000003.12:g.425
    39280_42549641inv
    GRCh38 (hg38)NC_000003.12Chr342,539,28042,549,641
    nssv18771276RemappedPerfectNC_000003.11:g.425
    80772_42591133inv
    GRCh37.p13First PassNC_000003.11Chr342,580,77242,591,133

    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)
    nssv187712761.8e-055274746
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