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nsv7028619

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,040

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 129 SVs from 24 studies. See in: genome view    
    Submitted genomic43,922,512-43,925,551Question Mark
    Overlapping variant regions from other studies: 129 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):42,551,152-42,554,191Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7028619Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2043,922,51243,925,551
    nsv7028619RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2042,551,15242,554,191

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431820deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431820Submitted genomicNC_000020.11:g.439
    22512_43925551del
    GRCh38 (hg38)NC_000020.11Chr2043,922,51243,925,551
    nssv18431820RemappedPerfectNC_000020.10:g.425
    51152_42554191del
    GRCh37.p13First PassNC_000020.10Chr2042,551,15242,554,191

    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)
    nssv184318204e-061275988
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