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nsv6670838

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,853

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 32 studies. See in: genome view    
    Submitted genomic219,950,464-219,953,316Question Mark
    Overlapping variant regions from other studies: 163 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):220,123,806-220,126,658Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6670838Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1219,950,464219,953,316
    nsv6670838RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1220,123,806220,126,658

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18367520deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18367520Submitted genomicNC_000001.11:g.219
    950464_219953316de
    l
    GRCh38 (hg38)NC_000001.11Chr1219,950,464219,953,316
    nssv18367520RemappedPerfectNC_000001.10:g.220
    123806_220126658de
    l
    GRCh37.p13First PassNC_000001.10Chr1220,123,806220,126,658

    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)
    nssv18367520<0.001120253504
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