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nsv6674303

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 30 studies. See in: genome view    
    Submitted genomic235,622,001-235,627,500Question Mark
    Overlapping variant regions from other studies: 177 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):235,785,301-235,790,800Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6674303Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1235,622,001235,627,500
    nsv6674303RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1235,785,301235,790,800

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18370610deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18370610Submitted genomicNC_000001.11:g.235
    622001_235627500de
    l
    GRCh38 (hg38)NC_000001.11Chr1235,622,001235,627,500
    nssv18370610RemappedPerfectNC_000001.10:g.235
    785301_235790800de
    l
    GRCh37.p13First PassNC_000001.10Chr1235,785,301235,790,800

    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)
    nssv18370610<0.001186250994
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