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nsv6832204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,957

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 22 studies. See in: genome view    
    Submitted genomic38,614,355-38,616,311Question Mark
    Overlapping variant regions from other studies: 82 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):38,653,955-38,655,911Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6832204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr738,614,35538,616,311
    nsv6832204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr738,653,95538,655,911

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18541578deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18541578Submitted genomicNC_000007.14:g.386
    14355_38616311del
    GRCh38 (hg38)NC_000007.14Chr738,614,35538,616,311
    nssv18541578RemappedPerfectNC_000007.13:g.386
    53955_38655911del
    GRCh37.p13First PassNC_000007.13Chr738,653,95538,655,911

    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)
    nssv18541578<0.001224274842
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