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nsv7052507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:98

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 105 SVs from 18 studies. See in: genome view    
    Submitted genomic109,406,043-109,406,140Question Mark
    Overlapping variant regions from other studies: 105 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):109,727,246-109,727,343Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7052507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,406,043109,406,140
    nsv7052507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,727,246109,727,343

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18776609inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18776609Submitted genomicNC_000006.12:g.109
    406043_109406140in
    v
    GRCh38 (hg38)NC_000006.12Chr6109,406,043109,406,140
    nssv18776609RemappedPerfectNC_000006.11:g.109
    727246_109727343in
    v
    GRCh37.p13First PassNC_000006.11Chr6109,727,246109,727,343

    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)
    nssv18776609<0.00167275034
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