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nsv6546109

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:644

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 159 SVs from 29 studies. See in: genome view    
    Submitted genomic31,664,226-31,664,869Question Mark
    Overlapping variant regions from other studies: 159 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):33,036,539-33,037,182Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6546109Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2131,664,22631,664,869
    nsv6546109RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2133,036,53933,037,182

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18206066duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18206066Submitted genomicNC_000021.9:g.3166
    4226_31664869dup
    GRCh38 (hg38)NC_000021.9Chr2131,664,22631,664,869
    nssv18206066RemappedPerfectNC_000021.8:g.3303
    6539_33037182dup
    GRCh37.p13First PassNC_000021.8Chr2133,036,53933,037,182

    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)
    nssv18206066<0.001238588
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