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nsv6618220

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,677

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 27 studies. See in: genome view    
    Submitted genomic138,748,589-138,754,265Question Mark
    Overlapping variant regions from other studies: 125 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):139,069,726-139,075,402Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6618220Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6138,748,589138,754,265
    nsv6618220RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6139,069,726139,075,402

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18216862duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18216862Submitted genomicNC_000006.12:g.138
    748589_138754265du
    p
    GRCh38 (hg38)NC_000006.12Chr6138,748,589138,754,265
    nssv18216862RemappedPerfectNC_000006.11:g.139
    069726_139075402du
    p
    GRCh37.p13First PassNC_000006.11Chr6139,069,726139,075,402

    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)
    nssv18216862<0.001639288
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