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nsv6329021

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:267,036

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 915 SVs from 67 studies. See in: genome view    
    Submitted genomic99,682,330-99,949,365Question Mark
    Overlapping variant regions from other studies: 915 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):100,147,886-100,414,921Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6329021Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr199,682,33099,949,365
    nsv6329021RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1100,147,886100,414,921

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18202145duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18202145Submitted genomicNC_000001.11:g.996
    82330_99949365dup
    GRCh38 (hg38)NC_000001.11Chr199,682,33099,949,365
    nssv18202145RemappedPerfectNC_000001.10:g.100
    147886_100414921du
    p
    GRCh37.p13First PassNC_000001.10Chr1100,147,886100,414,921

    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)
    nssv18202145<0.001439264
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