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nsv7046721

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:130

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 144 SVs from 18 studies. See in: genome view    
    Submitted genomic165,988,702-165,988,831Question Mark
    Overlapping variant regions from other studies: 144 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):166,402,190-166,402,319Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046721Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6165,988,702165,988,831
    nsv7046721RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6166,402,190166,402,319

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777685inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777685Submitted genomicNC_000006.12:g.165
    988702_165988831in
    v
    GRCh38 (hg38)NC_000006.12Chr6165,988,702165,988,831
    nssv18777685RemappedPerfectNC_000006.11:g.166
    402190_166402319in
    v
    GRCh37.p13First PassNC_000006.11Chr6166,402,190166,402,319

    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)
    nssv187776854e-061276268
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