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nsv7032945

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:332,254

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1264 SVs from 70 studies. See in: genome view    
    Submitted genomic31,283,144-31,615,397Question Mark
    Overlapping variant regions from other studies: 1257 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):29,870,947-30,203,200Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7032945Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2031,283,14431,615,397
    nsv7032945RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2029,870,94730,203,200

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18643507duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18643507Submitted genomicNC_000020.11:g.312
    83144_31615397dup
    GRCh38 (hg38)NC_000020.11Chr2031,283,14431,615,397
    nssv18643507RemappedPerfectNC_000020.10:g.298
    70947_30203200dup
    GRCh37.p13First PassNC_000020.10Chr2029,870,94730,203,200

    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)
    nssv186435074e-061275538
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