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nsv6829600

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,246

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 187 SVs from 47 studies. See in: genome view    
    Submitted genomic100,591,618-100,623,863Question Mark
    Overlapping variant regions from other studies: 187 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):100,189,241-100,221,486Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6829600Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7100,591,618100,623,863
    nsv6829600RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7100,189,241100,221,486

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18716831duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18716831Submitted genomicNC_000007.14:g.100
    591618_100623863du
    p
    GRCh38 (hg38)NC_000007.14Chr7100,591,618100,623,863
    nssv18716831RemappedPerfectNC_000007.13:g.100
    189241_100221486du
    p
    GRCh37.p13First PassNC_000007.13Chr7100,189,241100,221,486

    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)
    nssv187168314e-061273860
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