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nsv6542619

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,415

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 406 SVs from 47 studies. See in: genome view    
    Submitted genomic30,361,296-30,455,710Question Mark
    Overlapping variant regions from other studies: 406 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):31,733,614-31,828,028Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6542619Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2130,361,29630,455,710
    nsv6542619RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2131,733,61431,828,028

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18069720deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18069720Submitted genomicNC_000021.9:g.3036
    1296_30455710del
    GRCh38 (hg38)NC_000021.9Chr2130,361,29630,455,710
    nssv18069720RemappedPerfectNC_000021.8:g.3173
    3614_31828028del
    GRCh37.p13First PassNC_000021.8Chr2131,733,61431,828,028

    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)
    nssv18069720<0.001139238
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