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nsv6924218

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,105,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3350 SVs from 88 studies. See in: genome view    
    Submitted genomic55,714,201-56,819,900Question Mark
    Overlapping variant regions from other studies: 3350 SVs from 88 studies. See in: genome view    
    Remapped(Score: Perfect):56,107,985-57,213,684Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6924218Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1255,714,20156,819,900
    nsv6924218RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,107,98557,213,684

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18595933duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18595933Submitted genomicNC_000012.12:g.557
    14201_56819900dup
    GRCh38 (hg38)NC_000012.12Chr1255,714,20156,819,900
    nssv18595933RemappedPerfectNC_000012.11:g.561
    07985_57213684dup
    GRCh37.p13First PassNC_000012.11Chr1256,107,98557,213,684

    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)
    nssv185959334e-061274448
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