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nsv6342429

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69,804

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 331 SVs from 55 studies. See in: genome view    
    Submitted genomic152,759,529-152,829,332Question Mark
    Overlapping variant regions from other studies: 331 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):153,616,043-153,685,846Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6342429Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2152,759,529152,829,332
    nsv6342429RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2153,616,043153,685,846

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205550duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205550Submitted genomicNC_000002.12:g.152
    759529_152829332du
    p
    GRCh38 (hg38)NC_000002.12Chr2152,759,529152,829,332
    nssv18205550RemappedPerfectNC_000002.11:g.153
    616043_153685846du
    p
    GRCh37.p13First PassNC_000002.11Chr2153,616,043153,685,846

    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)
    nssv18205550<0.001439288
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