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nsv7025533

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,430

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 199 SVs from 31 studies. See in: genome view    
    Submitted genomic42,683,854-42,687,283Question Mark
    Overlapping variant regions from other studies: 200 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):44,103,964-44,107,393Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7025533Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2142,683,85442,687,283
    nsv7025533RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2144,103,96444,107,393

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436405deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436405Submitted genomicNC_000021.9:g.4268
    3854_42687283del
    GRCh38 (hg38)NC_000021.9Chr2142,683,85442,687,283
    nssv18436405RemappedPerfectNC_000021.8:g.4410
    3964_44107393del
    GRCh37.p13First PassNC_000021.8Chr2144,103,96444,107,393

    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)
    nssv184364054e-061276100
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