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nsv6554938

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 202 SVs from 33 studies. See in: genome view    
    Submitted genomic30,557,301-30,560,400Question Mark
    Overlapping variant regions from other studies: 202 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):31,929,620-31,932,719Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6554938Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2130,557,30130,560,400
    nsv6554938RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2131,929,62031,932,719

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18069727deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18069727Submitted genomicNC_000021.9:g.3055
    7301_30560400del
    GRCh38 (hg38)NC_000021.9Chr2130,557,30130,560,400
    nssv18069727RemappedPerfectNC_000021.8:g.3192
    9620_31932719del
    GRCh37.p13First PassNC_000021.8Chr2131,929,62031,932,719

    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)
    nssv18069727<0.001138964
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