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nsv6350272

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52,227

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 284 SVs from 34 studies. See in: genome view    
    Submitted genomic174,704,944-174,757,170Question Mark
    Overlapping variant regions from other studies: 284 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):175,569,672-175,621,898Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6350272Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2174,704,944174,757,170
    nsv6350272RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2175,569,672175,621,898

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18081396deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18081396Submitted genomicNC_000002.12:g.174
    704944_174757170de
    l
    GRCh38 (hg38)NC_000002.12Chr2174,704,944174,757,170
    nssv18081396RemappedPerfectNC_000002.11:g.175
    569672_175621898de
    l
    GRCh37.p13First PassNC_000002.11Chr2175,569,672175,621,898

    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)
    nssv18081396<0.001239258
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