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nsv6911180

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,647

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 141 SVs from 39 studies. See in: genome view    
    Submitted genomic56,483,334-56,512,980Question Mark
    Overlapping variant regions from other studies: 143 SVs from 39 studies. See in: genome view    
    Remapped(Score: Perfect):56,250,810-56,280,456Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6911180Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,483,33456,512,980
    nsv6911180RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1156,250,81056,280,456

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18575538duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18575538Submitted genomicNC_000011.10:g.564
    83334_56512980dup
    GRCh38 (hg38)NC_000011.10Chr1156,483,33456,512,980
    nssv18575538RemappedPerfectNC_000011.9:g.5625
    0810_56280456dup
    GRCh37.p13First PassNC_000011.9Chr1156,250,81056,280,456

    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)
    nssv185755384e-061274236
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