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nsv6425699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,554,401

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6389 SVs from 112 studies. See in: genome view    
    Submitted genomic82,628,086-85,182,486Question Mark
    Overlapping variant regions from other studies: 6400 SVs from 112 studies. See in: genome view    
    Remapped(Score: Perfect):83,540,321-86,094,721Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6425699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr882,628,08685,182,486
    nsv6425699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr883,540,32186,094,721

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18218899duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18218899Submitted genomicNC_000008.11:g.826
    28086_85182486dup
    GRCh38 (hg38)NC_000008.11Chr882,628,08685,182,486
    nssv18218899RemappedPerfectNC_000008.10:g.835
    40321_86094721dup
    GRCh37.p13First PassNC_000008.10Chr883,540,32186,094,721

    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)
    nssv18218899<0.001439188
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