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nsv6644103

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,019

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 274 SVs from 49 studies. See in: genome view    
    Submitted genomic166,565,301-166,613,319Question Mark
    Overlapping variant regions from other studies: 278 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):166,534,538-166,582,556Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644103Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1166,565,301166,613,319
    nsv6644103RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1166,534,538166,582,556

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18363976deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18363976Submitted genomicNC_000001.11:g.166
    565301_166613319de
    l
    GRCh38 (hg38)NC_000001.11Chr1166,565,301166,613,319
    nssv18363976RemappedPerfectNC_000001.10:g.166
    534538_166582556de
    l
    GRCh37.p13First PassNC_000001.10Chr1166,534,538166,582,556

    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)
    nssv18363976<0.00152274562
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