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nsv6341517

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:525

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 18 studies. See in: genome view    
    Submitted genomic174,761,445-174,761,969Question Mark
    Overlapping variant regions from other studies: 150 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):175,626,173-175,626,697Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6341517Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2174,761,445174,761,969
    nsv6341517RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2175,626,173175,626,697

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18081400deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18081400Submitted genomicNC_000002.12:g.174
    761445_174761969de
    l
    GRCh38 (hg38)NC_000002.12Chr2174,761,445174,761,969
    nssv18081400RemappedPerfectNC_000002.11:g.175
    626173_175626697de
    l
    GRCh37.p13First PassNC_000002.11Chr2175,626,173175,626,697

    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)
    nssv18081400<0.001135494
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