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nsv7025529

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:160

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 15 studies. See in: genome view    
    Submitted genomic34,491,638-34,491,797Question Mark
    Overlapping variant regions from other studies: 125 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):33,079,443-33,079,602Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7025529Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2034,491,63834,491,797
    nsv7025529RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2033,079,44333,079,602

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642060duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642060Submitted genomicNC_000020.11:g.344
    91638_34491797dup
    GRCh38 (hg38)NC_000020.11Chr2034,491,63834,491,797
    nssv18642060RemappedPerfectNC_000020.10:g.330
    79443_33079602dup
    GRCh37.p13First PassNC_000020.10Chr2033,079,44333,079,602

    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)
    nssv186420609e-062228040
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