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nsv7037706

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,214

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 206 SVs from 38 studies. See in: genome view    
    Submitted genomic42,140,452-42,147,665Question Mark
    Overlapping variant regions from other studies: 207 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):43,560,562-43,567,775Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7037706Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2142,140,45242,147,665
    nsv7037706RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2143,560,56243,567,775

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18438042deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18438042Submitted genomicNC_000021.9:g.4214
    0452_42147665del
    GRCh38 (hg38)NC_000021.9Chr2142,140,45242,147,665
    nssv18438042RemappedPerfectNC_000021.8:g.4356
    0562_43567775del
    GRCh37.p13First PassNC_000021.8Chr2143,560,56243,567,775

    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)
    nssv184380424e-061276254
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