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nsv7037740

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,914

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 688 SVs from 54 studies. See in: genome view    
    Submitted genomic20,768,467-20,772,380Question Mark
    Overlapping variant regions from other studies: 688 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):21,122,755-21,126,668Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7037740Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2220,768,46720,772,380
    nsv7037740RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2221,122,75521,126,668

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18438528deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18438528Submitted genomicNC_000022.11:g.207
    68467_20772380del
    GRCh38 (hg38)NC_000022.11Chr2220,768,46720,772,380
    nssv18438528RemappedPerfectNC_000022.10:g.211
    22755_21126668del
    GRCh37.p13First PassNC_000022.10Chr2221,122,75521,126,668

    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)
    nssv184385281.1e-053274832
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