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nsv6347384

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 21 studies. See in: genome view    
    Submitted genomic210,021,201-210,022,600Question Mark
    Overlapping variant regions from other studies: 107 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):210,885,925-210,887,324Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6347384Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2210,021,201210,022,600
    nsv6347384RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2210,885,925210,887,324

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18085100deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18085100Submitted genomicNC_000002.12:g.210
    021201_210022600de
    l
    GRCh38 (hg38)NC_000002.12Chr2210,021,201210,022,600
    nssv18085100RemappedPerfectNC_000002.11:g.210
    885925_210887324de
    l
    GRCh37.p13First PassNC_000002.11Chr2210,885,925210,887,324

    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)
    nssv18085100<0.001138810
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