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nsv7035517

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 39 studies. See in: genome view    
    Submitted genomic31,544,310-31,544,418Question Mark
    Overlapping variant regions from other studies: 174 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):32,916,623-32,916,731Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7035517Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2131,544,31031,544,418
    nsv7035517RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2132,916,62332,916,731

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18436212deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18436212Submitted genomicNC_000021.9:g.3154
    4310_31544418del
    GRCh38 (hg38)NC_000021.9Chr2131,544,31031,544,418
    nssv18436212RemappedPerfectNC_000021.8:g.3291
    6623_32916731del
    GRCh37.p13First PassNC_000021.8Chr2132,916,62332,916,731

    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)
    nssv184362120.33686376255430
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