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nsv6864068

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,032

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 100 SVs from 20 studies. See in: genome view    
    Submitted genomic106,897,296-106,901,327Question Mark
    Overlapping variant regions from other studies: 100 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):109,659,577-109,663,608Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6864068Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9106,897,296106,901,327
    nsv6864068RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9109,659,577109,663,608

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18562006deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18562006Submitted genomicNC_000009.12:g.106
    897296_106901327de
    l
    GRCh38 (hg38)NC_000009.12Chr9106,897,296106,901,327
    nssv18562006RemappedPerfectNC_000009.11:g.109
    659577_109663608de
    l
    GRCh37.p13First PassNC_000009.11Chr9109,659,577109,663,608

    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)
    nssv185620064e-061275960
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